Abbott, M.E. and J. Kaufmann. 1916. Double monster of Janus type: cephalothoracopagus monosymmetros cyclops synotis. Bulletin of the International Association of Medical Museums 6: 95–101
Abramowicz, M.J. et al. 1992. Identification of a mutation in the coding sequence of the human thyroid peroxidase gene causing congenital goitre. Journal of Clinical Investigation 90: 1200–4
Abu-Abed, S. et al. 2001. The retinoic acid-metabolising enzyme CYP26A1, is essential for normal hindbrain patterning, vertebral identity and development of posterior structures. Genes and Development 15: 226–40
Addison, J. 1721. The battel [sic] of the pygmies and cranes. London
Adelmann, H.B. 1936a. The problem of Cyclopia I. Quarterly Review of Biology II: 161–82
Adelmann, H.B. 1936b. The problem of Cyclopia II. Quarterly Review of Biology 11: 284–304
Afzelius, B. 1976. A human syndrome caused by immotile cilia. Science 193: 317–19
Alberch, P. 1986. Possible dogs. Natural History 95: 4–8
Alberts, B. et al. 1994. The molecular biology of the cell. Garland, N.Y.
Albin, R.L. 1988. The pleiotropic gene theory of senescence: supportive evidence from human genetic disease. Ethology and Sociobiology 9: 371–82
Aldrovandi, U. 1642. Monstrorum historia. Bononiae
Ames, B.N. et al. 1993. Oxidants, antioxidants, and the degenerative diseases of ageing. Proceedings of the National Academy of Sciences, USA 90:7915–22
Anon. 1829a. Bulletin des sciences médicales 18: 169–72
Anon. 1829b. La Clinique 1: 200
Anon. 1829c. La Clinique 1: 254–5
Appel, T. 1987. The Cuvier–Geoffroy debate: French biology in the decade before Darwin Oxford University Press, Oxford, UK
Aristotle. 1984. The complete works of Aristotle: the revised Oxford translation J. Barnes (ed.) Princeton University Press, Princeton, N.J.
Aterman, K. 1999. From Horus the child to Hephaestus who limps: a romp through history. American Journal of Medical Genetics 83: 53–63
Bachiller, D. et al. 2000. The organiser factors chordin and noggin are required for mouse forebrain development. Nature 403: 658–61
Bacon, F. 1620 (2000). The new organon. L. Jardine and M. Silverthorne (eds) Cambridge Unversity Press, Cambridge, UK
Baker, J.R. 1974. Race. Oxford University Press, N.Y.
Balemans, W. et al. 2001. Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST). Human Molecular Genetics 10: 537–43
Baljet, B. 1990. The cyclopic monsters of the Vrolik collection. Actes du 5e colloque de conservateurs des musées d’histoire des sciences médicales 66–78.
Baljet, B. and M.L. Öjesjö. 1994. Teratology in art or the Dysmorphology–Hieronymus Bosch Connection. Actes du 7e colloque des conservateurs des musées d’histore des sciences médicales
Baljet, B. and R.–J. Oostra. 1998. Historical aspects of the study of malformations in the Netherlands. American journal of Medical Genetics 77: 91–9
Baljet, B. et al. 1991. Willem Vrolik on cyclopia. Documenta Opthalmologica 77: 355–68
Bamshad, M. et al. 1999. Reconstructing the history of human limb development: lessons from birth defects. Pediatric Research 45: 291–9
Barbin, H. 1980. Herculine Barbin: being the recently discovered memoirs of a nineteenth century French hermaphrodite (intro. M. Foucault, trans. R. McDougall). Pantheon, N.Y.
Barbujani, G. et al. 1997. An apportionment of human DNA diversity. Proceedings of the National Academy of Sciences USA 94 4516–19
Barinaga, M. 1993. New protein appears to be long-sought neural inducer. Science 262: 653–54
Barrett, D. and M. McCann. 1980. Two-toed man. Sunday Times Magazine 28–31
Barsh, G. 1999. Of ancient tales and hairless tails. Nature Genetics 22:315–16
Bartke, A. et al. 2001a. Longevity – extending the lifespan of long-lived mice. Nature 414: 412
Bartke, A. et al. 2001b. Prolonged longevity of hypopituitary dwarf mice. Experimental Gerontology 36: 21–8
Bates, A.W. 2001. The De monstrorum of Fortunio Liceti: a landmark of descriptive teratology. Journal of Medical Biography 9: 49–54
Bateson, W. 1894. Materials for the study of variation. Macmillan, London
Bazopoulou-Kyrkanidou, E. 1997. What makes Hephaestus lame? American Journal of Medical Genetics 72: 144–55
Beckman, K.B. and B.N. Ames. 1998. The free radical theory of ageing matures. Physiological Reviews 78: 547–81
Beddington, R.S.P. 1994. Induction of a second neural axis by the mouse node. Development 120: 613–20
Beddington, R.S.P. and E.J. Robertson. 1999. Axis development and early asymmetry in mammals. Cell 96: 195–209
Bell, A.G. 1918. The duration of life and conditions associated with longevity. Genealogical Record Office, Washington, DC
Bendyshe, T. 1864. On the anthropology of Linnaeus. Memoires of the Anthropological Society of London 1: 421–58
Besser, G.M. and M.O. Thorner. 1994. Clinical endocrinology (2nd ed.) Ch. 11. Mosby-Wolfe, London
Betts, D.H. et al. 2001. Reprogramming of telomerase activity and rebuilding of telomere length in cloned cattle. Proceedings of the National Academy of Sciences, USA 98: 1077–82
Bindman, D. 2002. Ape to Apollo: aesthetics and the idea of race in the eighteenth century. Reaktion, London
Birkett, J. 1858. Congential, supernumerary and imperfectly developed auricles on the sides of the neck. Transactions of the Pathological Society of London 9: 448–9
Bittles, A.H. 2001. Consaguinity and its relevance to clinical genetics Clinical Genetics 60: 89–90
Blair, H.C. 1998. How the osteoclast degrades bone. Bioessays 20: 837–46
Blanchard, R. 1907. Nouvelles observations sur les nègres pies. Geoffroy Satin-Hilaire à Lisbonne. Bulletin de la Société Française d’histoire de la médecine 6: 111–35
Blasco, M.A. et al. 1997. Telomere shortening and tumor formation by mouse cells lacking telomerase RNA. Cell 91: 25–34
Boaistuau, P. 1560 (2000) Histoires prodigieuses, Facsimile of Wellcome MS 136.XS. Bamforth ed.) Franco Maria Ricci, Milan
Boardman, J. 1997a. Pan in text pp.923–41; plate pp.612–36 in Lexicon iconographicum mythologiae classicae: VIII: 1 (text); 2 (Plates)
Boardman, J. 1997b. The great god Pan. Thames and Hudson, London
Boas, F. 1912. Changes in bodily form of descendants of immigrants. American Anthropologist 14: 530–62
Bodnar, A.G. et al. 1998. Extension of life-span by introduction of telomerase into normal human cell. Science 279: 349–51
Bogin, B. 1999. Patterns of human growth, 2nd ed. Cambridge University Press, Cambridge. UK
Bonaventure, J. et al. 1996. Common mutations in the Fibroblast Growth Factor Receptor 3 (FGFR3) gene account for achondroplasia, hypochondroplasia and thanatophoric dwarfism. American Journal of Medical Genetics 63: 148–54
Bondeson, J. 1997. A cabinet of medical curiosities. Tauris, London
Bondeson, J. 2000. The two-headed boy and other medical marvels. Cornell University Press, Ithaca. N.Y.
Bondeson, J. and A.E.W. Miles. 1996. The hairy family of Burma: a four generation pedigree of congenital hypertrichosis lanuginosa. Journal of the Royal Society of Medicine 89: 403–8
Bornstein, P.E. and R.R. Peterson. 1966. Numerical variation in the pre-sacral vertebral column in three population groups. American Journal of Physical Anthropology 25: 139–46
Boruwlaski, J. 1792. The Memoirs of the celebrated dwarf, Joseph Boruwlasty, A Polish gentleman containing a faithful and curious account of his birth, education, marriage, travels and voyages. (trans. S. Freeman) 2nd ed. J. Thompson. Birmingham
Boulet and Capecchi. 1996. Targeted disruption of Hoxc-4 causes esophageal defects and vertebral transformation. Developmental Biology 177: 232–49
Boyd, W.C. 1955. Genetics and the races of man. Little, Brown and Co., Boston
Brandt, A. 1897. Üeber die sogenannten Hundemenschen, beziehungsweise über Hypertrichosis universalis. Biologische Zentralblatt 17: 161–79
Broberg, G. 1983. Homo sapiens. Linnaeus’ classification of man. in T. Frangsmyr, (ed.) Linnaeus: the man and his work. University of California Press, Berkley
Brockes, J.P. 1998. Regeneration and cancer. Biochimica et biophysica acta. 1377 M1-M11
Brown-Borg, H.M. et al. 1996. Dwarf mice and ageing process. Nature 384: 33
Browne, T. 1904. The works of Thomas Browne. C. Sayle (ed.) Grant Richards, London
Brueckner, M. 2001. Cilia propel the embryo in the right direction. American Journal of Medical Genetics 101: 339–44
Brunet, L.J. et al. 1998. Noggin, cartilage morphogenesis, and joint formation in the mammalian skeleton. Science 280: 1455–7
Brunkow, M.E. et al. 2001. Bone dysplasia sclerosteosis results from loss of the SOST gene product, a novel cystine knot-containing protein. American Journal of Human Genetics 68: 577–89
Bruyn, G.W. and L.N. Went 1986. Huntington’s Chorea, in Vinken, G. W. et al. (eds.) Extrapyramidal disorders: handbook of clinical neurology 49: 267–73
Buffon, G.L. 1777. Histoire naturelle générale et particulière. Imprimerie Royale, Paris
Burn, J. and T. Strachan. 1995. Human embryo use in developmental research. Nature Genetics 11: 3–6
Callahan, C.A. and A.E. Oro. 2001. Monstrous attempts at adnexogenesis: regulating hair follicle progenitors through sonic hedgehog signalling. Current Opinion in Genetics and Development 11: 541–6
Cargill, M. et al. 1999. Characterisation of single-nucleotide polymorphisms in coding regions of human genes. Nature Genetics 22: 231–8
Carpenter, E.M. et al. 1993. Loss of Hox-Ai (Hox-1. 6) function results in the reorganisation of the murine hindbrain. Development 118: 1063–75
Casey, B. and B.P. Hackett. 2000. Left–right axis malformations in man and mouse. Current Opinon in Genetics and Development 10: 257–61
Cavalli-Sforza, L.L. 1986. The African pygmies. Academic Press, N.Y.
Cavelaars, A.E.J.M. et al. 2000. Persistent variations in average height between countries and between socio-economic groups: an overview of 10 European countries Annals of Human Biology 27: 407–21
Celli, J. et al. 1999. Heterozygous germline mutations in the P53 homolog P63 are the cause of EEC syndrome. Cell 99: 143–51
Chapman, T. and L. Partridge. 1996. Female fitness in Drosophila melanogaster: an interaction between the effect of nutrition and of encounter rates with males. Proceedings of the Royal Society, London Series B Biological Sciences 263: 755–9
Charlesworth, B. 1996. Evolution of senescence: Alzheimer’s disease and evolution. Current Biology 6: 20–2
Chen, L. et al. 2001. A Ser(365)->Cys mutation of fibroblast growth factor receptor 3 in mouse downregulates Ihh/PTHrP signals and causes severe achondroplasia. Human Molecular Genetics 10: 457–65
Chen, Y. et al. 2000. Conservation of early odontogenetic signaling pathways in Aves. Proceedings of the National Academy, USA 97: 10044–9
Chiang, C. et al. 1996. Cyclopia and defective axial patterning in mice lacking sonic hedgehog gene function. Nature 383: 407–12
Chiang, C. et al. 2001. Manifestation of the limb prepattern: limb development in the absence of sonic hedgehog function. Developmental Biology 236: 421–35
Chisaka, O. and M.R. Capecchi. 1991. Regionally restricted developmental defects resulting from targeted disruption of the mouse homeobox gene hox-i. 5 (HoxA3). Nature 350: 473–9
Cibelli, J.B. et al. 2002. The health profile of cloned animals. Nature Biotechnology 20: 13–14
Clark, R.M. et al. 2001. Reciprocal mouse and human limb phenotypes caused by gain and loss-of-function mutations affecting Lmbri. Genetics 159: 715–26
Coates, M.I. and J.A. Clack. 1990. Polydactyly in the earliest tetrapod limbs. Nature 347: 66–9
Cockayne, E.A. 1933. Inherited abnormalities of the skin and its appendages. Oxford University Press, London
Cohen, M.M. 2002. Bone morphogenetic proteins with some comments on fibrodysplasia ossificans progressiva. American Journal of Medical Genetics 109: 87–92
Cohen, M.M. 1988. Further diagnostic thoughts about the Elephant Man. American Journal of Medical Genetics 29: 777–82
Cohen, M.M. 1989. A comprehensive and critical assessment of overgrowth and overgrowth syndromes. Advances in Human Genetics 18: 181–303
Cohen, M.M. 1993. Proteus syndrome: clinical evidence for somatic mosaicism and selective review. American Journal of Medical Genetics 47: 645–52
Cohen, M.M. 2001. Problems in the definition of holoprosencephaly. American Journal of Medical Genetics 103: 183–7
Cohen, M.M. and K. Shiota. 2002. Teratogenesis of holoprosencephaly. American Journal of Medical Genetics 109: 1–15
Cohn, M.J. and C. Tickle. 1999. Developmental basis for limblessness and axial patterning in snakes. Nature 399: 474–9
Cohn, M.J. and P.E. Bright. 2000. Development of vertebrate limbs: insight into pattern, evolution and dysmorphogenesis. in O’Higgins, P. and M.J. Cohn (eds) Development, growth and evolution: implications for the hominid skeleton. Academic Press, N.Y.
Collins-Schramm, H.E. 2002. Ethnic-difference markers for use in mapping by admixture linkage disequilibrium. American Journal of Human Genetics 70: 737–50
Colvin, J.S. et al. 1996. Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3. Nature Genetics 12: 391–7
Comfort, A. 1964. Ageing: the biology of senesence. Holt, Rinehart and Winston. N.Y.
Conner, M. and M. Ferguson-Smith. 1993. Essentials of medical genetics. (5th ed.) Blackwell Science, Oxford
Conte, F. A. et al. 1994. A syndrome of female pseudohermaphroditism, hypergonadotropic hypogonadism, and multicystic ovaries associated with missense mutations in the gene encoding aromatase (P450 arom). Journal of Clinical Endocrinology and Metabolism 78: 1287–92
Corcoran, J. 1998. What are the molecular mechanims of neural tube defects? Bioessays 20: 6–8
Corder, E.H. et al. 1993. Gene dose of apololipoprotein E Type 4 allele and the risk of Alzheimer’s disease in late onset families. Science 261: 921–3
Cornaro, L. 1550 (1903). The art of living long: a new and improved English version of the treatise by the celebrated Venetian centenarian, Louis Cornaro with Essays by Joseph Addison, Lord Bacon and Sir William Temple. W.F. Butler, Milwaukee
Cotsarelis, G. and S.E. Millar. 2001. Towards a molecular understanding of hair loss and its treatment. Trends in Molecular Medicine 7: 293–301
Crackower, M.A. et al. 1998. Defect in the maintenance of the apical ectodermal ridge in the Dactylaplasia mouse. Developmental Biology 201: 78–89
Crawfurd, J. 1827. Journal of an embassy from the Governor-General of India to the court of Ava in the year 1827. V.i.H. Colburn. London
Crosby, J.L. et al. 1992. Disorganisation is a completely dominant gain-of-function mouse mutation causing sporadic developmental defects. Mechanisms of Development 37: 121–6
Crow, J.F. 2000. The origins, patterns and implications of human spontaneous mutation. Nature Reviews Genetics 1: 40–7
Danerow, H. 1830. Ueber Ritta-Christina und die Siamesen. Litterarishcen Annaleen der gesammten Heilfyunde 16: 454–82
Darwin, C. 1859 (1968). The origin of species by means of natural selection. Penguin, Harmondsworth, UK
Darwin, C. 1871 (1981). The descent of man, and selection in relation to sex. Princeton University Press, Princeton, N.J.
Darwin, C. 1882. The variation of animals and plants under domestication, 2nd ed. John Murray, London
Dasen, V. 1993. Dwarfs in ancient Egypt and Greece. Clarendon Press, London
Dasen, V. 1994. Pygmaioi. text pp.594–601; plates pp.466–86. Lexicon Iconographicum Mythologiae Classicae VIII: 1 (text); 2 (plates)
Dasen, V. 1997. Multiple births in Graeco–Roman antiquity. Oxford Journal of Archaeology 16: 49–61
Dasen, V. 2002. Les jumeaux siamois dans l’Antiquité classique: du mythe au phénoméne de foire. La Revue du Practicien 52: 9–12
Daston, L. and K. Park. 1998. Wonders and the order of nature 1150–1750. Zone, N.Y.
De Luca, F. and J. Baron. 1999. Control of bone growth by fibroblast growth factors. Trends in Endocrinology and Metabolism 10: 61–5
De Quatrefages, A. 1895. The pygmies (trans. F. Starr). Macmillan, London
De Vijlder, J. et al. 1999. Defects in thyroid hormone supply. Ch. 16b. The Thyroid and Its Diseases. http://www.thyroidmanager.org
Del Campo, M. et al. 1999. Mondactylous limbs and abnormal genitalia are associated with hemizygosity for the human 2q31 region that includes the HOXD cluster. American Journal of Human Genetics 65: 104–10
Delange, F. and B. Hetzel. 2000. The Iodine Deficiency Disorders. Ch. 20. The Thyroid and Its Diseases. http://www.thyroidmanager.org
DeRobertis, E. and Y. Sasai. 1996. A common plan for dorsoventral patterning in Bilateria. Nature 380: 37–40
Diamond, J.M. 1982. Big-bang reproduction and ageing in male marsupial mice. Nature 298: 115–16
Diamond, J.M. 1991. Why are pygmies so small? Nature. 354: 111–12
Didde, R. 2002. Wetenschap. Volkskrant 25 May 2002
Dikötter, F. 1992. The discourse of race in modern China. Hurst, London
Dikötter, F 1997. Hairy barbarians, furry primates, and wild men: medical science and cultural representations of hair in China. in Hiltebeitel, A. and B. D. Miller (eds) Hair: its power and meaning in Asian cultures. SUNY Press, Albany, N.Y.
Dikötter, F. 1998. Imperfect conceptions: medical knowledge, birth defects, and eugenics in China. Hurst, London
Dobson, J. 1958. Marie Sabina, the variegated damsel. Annals of the Royal College of Surgeons 22: 273–8
Dollé, P. et al. 1993. Disruption of the Hoxd-13 gene induces localised heterochrony leading to mice with neotenic limbs. Cell 75: 431–41
Donnai D and R.M. Winter 1989. Disorganisation: a model for ‘early amnion rupture’? Journal of Medical Genetics 26: 421–5
Dreger, A.D. 1998. Hermaphrodites and the medical invention of sex. Harvard University Press. Cambridge, Mass.
Dudley, A.T. et al. 2002. A re-examination of proximodistal patterning during vertebrate development. Nature 418: 539–44
Durham-Pierre, D. et al. 1994. African origin of an intragenic deletion of the human P gene in tyrosine positive oculocutaneous albinism. Nature Genetics 7: 176–9
Egenvall, A. et al. 2000. Age pattern of mortality in eight breeds of insured dogs in Sweden. Preventative Veterinary Medicine 46: 1–14
Eigenmann, J.E. 1987. Insulin-like growth factor 1 in dogs. Frontiers of Hormone Research 17: 161–72
Eigenmann, J.E. et al. 1988. Insulin-like growth factor 1 levels in proportionate dogs, chondrodystrophic dogs and in giant dogs. Acta Endocrinologica (Copenhagen) 118: 105–8
Eigenmann, J.E. et. al. 1984. Body size parallels insulin-like growth factor 1 levels but not growth hormone secretory capacity. Acta Endocrinologica (Copenhagen) 106: 448–53
Emery, A.E.H. 1996. Genetic disorders in portraits. American Journal of Medical Genetics 66: 334–9
Epstein, C.J. et al. 1987. Transgenic mice with increased Cu/Zn-superoxide dismutase activity: animal model of dosage effects in Down syndrome. Proceedings of the National Academy of Sciences USA 84: 8044–8
Eyre-Walker, A. and P.D. Keightley. 1999. High genomic deleterious mutation rates in hominids. Nature 397: 334–47
Farrell, H.B. 1984. The two-toed Wadoma – familial ectrodactyly in Zimbabwe. South African Journal of Medicine 65: 531–3
Fãsseler, P.E. and K. Sander. 1996. Hilde Mangold (1898–1924) and Spemann’s organiser: Achievement and Tragedy. Wilhelm Roux Archives of Developmental Biology 205: 323–32
Felgenhauer, W.–R. 1969. Hypertrichosis lagnuinosa universalis. Journal de Génétique humaine 17: 1–44
Ferretti, P. and C. Tickle. 1997. The limbs, in P. Thorogood (ed.) Embryos, genes and birth defects. John Wiley and Sons, N.Y.
Figuera, L.E. 1995. Mapping of the congenital generalised hypertrichosis locus to chromosome Xq24-q27. 1. Nature Genetics 10: 202–6
Finch, C.E. 1990. Longevity, senescence and the genome. Chicago University Press
Finch, C.E. and G. Ruvkun. 2001. The genetics of ageing. Annual Reviews of Genomics and Human Genetics 2: 435–62
Fischer, J.L. 1972. Le concept experimental dans l’oeuvre tératologique d’Etienne Geoffroy Saint-Hilaire. Revue d’histoire des sciences 25: 347–62
Fischer, J.L. 1991. Monstres: histoire du corps et de ses défauts. Syros, Paris
Flanagan, N. et al. 2000. Pleiotropic effects of the melanocortin 1 receptor (MC1R) gene on human pigmentation. Human Molecular Genetics. 9: 2531–7
Flatt, A.E. 1994. The care of congenital hand anomalies. Quality Medical Publishing. St Louis. Mo.
Fleischer, R. 1984. Artemis Ephesia. text pp.755–63; plates pp.564–73 in Lexicon iconographicum mythologiae classicae II: 1 (text); 2 (plates)
Flurkey, K. et al. 2001. Lifespan extension and delayed immune and collagen aging in mutant mice with defects in growth hormone production. Proceedings of the National Academy of Sciences USA 98: 6736–41
Forbes, L.S. 1997. The evolutionary biology of spontaneous abortion in humans. Trends in Ecology and Evolutionary Biology 12: 446–50
Frank, L.G. 1997. Evolution of genital masculinisation: why do female hyenas have such a large ‘penis’? Trends in Ecology and Evolution 12:58–62
Frankcom, G. and J.H. Musgrave. 1976. The Irish giant. Duckworth, UK
Fraser, G. 1877. Wigtown and Whithorn: historical and descriptive sketches, stories and anecdotes, illustrative of the racy wit and pawky humour of the district. Gordon Fraser, Wigtown
Fraumeni, J.F 1967. Stature and malignant tumors of bone in childhood and adolesence. Cancer 20: 967–73
Freire-Maia, A. 1975. Genetics of acheiropodia (the handless and footless families of Brazil). VI. Formal genetic analysis. American Journal of Human Genetics 27: 521–7
Freire-Maia, A. 1981. Historical note: The extraordinary handless and footless families of Brazil – 50 years of acheiropodia. American Journal of Human Genetics 9: 31–41
Frey, J. 1994. Toulouse-Lautrec: a life. Weidenfeld and Nicolson, London
Frey, J. 1995a. What dwarfed Toulouse-Lautrec? Nature Genetics 10: 128–30
Frey, J. 1995b. Toulouse-Lautrec’s diagnosis – reply. Nature Genetics 11: 363
Friedman, J.B. 1981. The monstrous races in medieval thought and art. Harvard, Cambridge, Mass.
Fromental-Ramain, C. et al. 1996. Hoxa-13 and Hoxd-13 play a crucial role in the patterning of the autopod. Development 122: 2997–3011
Fullerton, S.M. et al. 2000. Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism. American Journal of Human Genetics 67: 881–900
Galis, F. 1999. Why do almost all mammals have seven cervical vertebrae? Developmental constraints, Hox genes, and Cancer. Journal of Experimental Zoology 285: 19–26
Galis, F. 2001. Why five fingers? Evolutionary constraints on digit number. Trends in Ecology and Evolution. 16: 637–46
Garcia-Cruz D. et al. 2002. Inherited hypertrichoses. Clinical Genetics 61: 321–9
Gat, U. et al. 1998. De novo hair follicle morphogenesis and hair tumors in mice expressing a truncated Beta-catenin in skin. Cell 95: 605–14
Gates, R.R. 1961. The Melanesian dwarf tribe of Aiome, New Guinea. Acta Geneticae Medicae et Gemellogiae. 10: 277–311
Geffner, M.E. et al. 1995. Insulin-like growth factor 1 resistance in immortalised T cell lines from African Efe pygmies. Journal of Clinical Endocrinology and Metabolism. 80: 3732–8
Geffner, M.E. et al. 1996. IGF-1 does not mediate T lymphoblast colony formation in response to estradiol, testosterone, 1,25(OH)2, Vitamin D3 and triiodothyronine; studies in control and pygmy lines Biochemical and Molecular Medicine 59: 72–9
Gegenbauer, C. 1880. Critical remarks on polydactlyly as atavism. Morphologisches Jahrbuch 6: 584–96
Gehring, W. and K. Ikeo. 1999. Pax 6: mastering eye morphogenesis and eye evolution. Trends in Genetics 15: 371–7
Geissler, W. et al. 1994. Male pseudohermaphroditism caused by mutations of testicular 17beta-hydroxysteroid dehydrogenase 3. Nature Genetics 7: 35–9
Gelb, D. et al. 1996. Pycnodysostosis, a lysosomal disease caused by Cathepsin K deficiency. Science 273: 1236–9
Gelfland, M., C.J. Roberts, and R.S. Roberts. 1974. A two-toed man from the Doma people of the Zambezi Valley. Rhodesian History 5: 92–5
Geoffroy Saint-Hilaire, E. 1822. Philosophic anatomique des monstruosités humaines. Deville-Cavellin, Paris
Geoffroy Saint-Hilaire, E. 1829. Rapport sur le monstre bicéphale Ritta-Christina. Gazette de Santé (No. 270)
Geoffroy Saint-Hilaire, E. 1838. Notions synthétiques, historiques et physi-ologiques de Philosophic Naturelle. Dénain, Paris
Geoffroy Saint-Hilaire, I. 1832–37. Histoire générale et particuliére des anomalies de l’organisation chez I’homme et les animaux. J. B. Balliére, Paris
Geoffroy Saint-Hilaire, I. 1847. Vie, travaux et doctrine scientifique d’Étienne Geoffroy Saint-Hilaire. La Société Géologique de France, Paris
Gerhart, J. 2000. Inversion of the chordate body axis: Are their alternatives? Proceedings of the National Academy of Sciences, USA 97: 4445–8
Gertz, O. 1948. Artemis och hinden frontispisplanschen Linnes Fauna Svecica. Svenska Linne-Sallskapets Arsskrift 31: 13–37
Gilbert, S.F. 2000. Developmental biology (6th edition). Sinauer Associates, Sunderland, Mass.
Glass, B. 1947. Maupertuis and the beginning of genetics. Quarterly Review of Biology 22: 196–210
Glickman, S.E. et al. 1992. Hormonal correlates of ‘masculinisation’ in female spotted hyenas (Crocuta crocuta). 1. Infancy to sexual maturity. Journal of Reproduction and Fertility 95: 451–62
Goding, C.R. 2000. Mitf from neural crest to melanoma: signal transduction and transcription in the melanocyte lineage. Genes and Development 14: 1712–28
Gong, Y. et al. 1999. Heterozygous mutations in the gene encoding noggin affect human morphogenesis. Nature Genetics 21: 302–4
Goto, N. et al. 1987. The mexican hairless dog, its morphology and inheritance. Experimental Animals (Tokyo) 36: 87–90
Goujon, E. 1869. Étude d’un cas d’hermaphrodisme bisexuel imparfait chez l’homme. Journal de I’anatomie et de la physiologie normales et pathologiques de l’homme et des animaux 6: 599–616
Gould, G.M. and W. L. Pyle. 1897. Anomalies and curiosities of medicine. W.B. Saunders, Philadelphia
Gould, S.J. 1981. The mismeasure of man. W.W. Norton, N.Y.
Gould, S.J. 1983. Hen’s teeth and horse’s toes. W.W. Norton, N.Y.
Graves, J.A. 1998. Interactions between SRY and SOX genes in mammalian sex determination. Bioessays 20: 264–9
Gravlee, C.G. et al. 2003. Heredity, environment and cranial form: a reanalysis of Boas’s Immigrant data. American Anthropologist 105: 125–38
Gruber, G.B. 1955. Historisches und aktuelles über das Sirenen-problem in der medizin. Nova Acta Leopoldina 17: 89–122
Gruman, G.J. 1966. A history of ideas about the prolongation of life. Transactions of the American Philosophical Society 56: 1–102
Gubbay, J. et al. 1990. A gene mapping to the sex-determining region of the mouse Y chromosome is a member of a novel family of embryonically expressed genes. Nature 346: 245–50
Guichard, C. et al. 2001. Axonemal dynein intermediate-chain gene (DNAI1) mutations result in situs inversus and primary ciliary dyskinesia (Kartagener syndrome). American Journal of Human Genetics 68: 1030–5
Günther, T. and T. Schinke. 2000. Mouse genetics have uncovered new paradigms in bone biology. Trends in Metabolism. 11: 189–93
Guyda, H.J. 1998. Growth hormone therapy for non-growth hormone-deficient children with short stature. Current Opinion in Pediatrics 10: 416–21
Haldane, J.B.S. 1941. New paths in genetics. George Allen & Unwin, London
Hale, F. 1933. Pigs born without eyeballs. Journal of Heredity 24: 105–6
Haliburton, R.G. 1891. The dwarfs of Mount Atlas. David Nutt, London
Haliburton, R.G. 1894. Survivals of dwarf races in the new world. Proceedings of the American Association for the Advancement of Science 14: 1–14
Hall, B.K. 1995. Atavisms and atavistic mutations. Nature Genetics 10: 126–7
Hamburger, V. 1947. Monsters in nature. Ciba Symposia 9: 666–83
Hamburger, V. 1988. The heritage of experimental embryology: Hans Spemann and the organiser. Oxford University Press
Hamilton, J.B. 1942. Male hormone stimulation is a prerequisite and an incitant in common baldness. American Journal of Anatomy 71: 451–80
Hanihara, T. 2000. Frontal and facial flatness of major human populations. American Journal of Physical Anthropology 111: 105–34
Haraguchi, R. et al. 2000. Molecular analysis of external genitalia formation: the role of fibroblast growth factor (FGF) genes during genital tubercle formation. Development 127: 2471–9
Harding, R.M. et al. 2000. Evidence for variable selective pressure at MC1R. American Journal of Human Genetics 66: 1351–61
Hardy, M.H. 1992. The secret life of the hair follicle. Trends in Genetics 8: 55–61
Harrison, R.G. 1924. Some unexpected results of the heteroplastic transplantation of limbs. Proceedings of the National Academy of Sciences, USA 10: 69–74
Harvey, R.G. and D.R. Brothwell. 1969. Biosocial aspects of Ainu hirsuteness. Journal of Biological Sciences 1: 109–24
Harvey, W. 1965. The works of William Harvey. Willis, R. (ed., trans.) Sydenham Society, London
Haupt, H. et al. 1990. he bestiaire de Rodolphe II. (trans. L. Marcou) Citadelles, Paris
Hayashizaki, Y. ef al. 1989. Thyroid-stimulating hormone (TSH) deficiency caused by a single base substitution in the CAGYC region of the ?-subunit. EMBO Journal 8: 2291–6
Headon, D.J. and P.A. Overbeek. 1999. Involvement of a novel Tnf receptor homologue in hair follicle induction. Nature Genetics 22: 370–4
Healy, E. et al. 2001. Functional variation of MC1R alleles from red-haired individuals. Human Molecular Genetics. 10: 2397–2402
Heijmans, B.T. et al. 2000. Common gene variants, mortality and extreme longevity in humans. Experimental Gerontology 35: 865–77
Hennessy, R.J. and C.B. Stringer. 2002. Geometric morphometric study of the regional variation of modern human craniofacial form. American Journal of Physical Anthropology 117: 37–48
Herdt, G. 1994. Mistaken sex: culture, biology and the third sex in New Guinea. in G. Herdt (ed.) Third sex, third gender. Zone Books. Cambridge, Mass.
Heron, T.M. 1986. Boruwlaski, the little count. Durham, UK
Hertel, C. 2001. Hairy issues: Portraits of Petrus Gonsalus and his family in Archduke Ferdinand IPs Kunstkammer and their contexts. Journal of the History of Collections 13: 1–22
Hinchliffe, J.R. and D.R. Johnson. 1980. The development of the vertebrate limb. Claredon Press, Oxford
Holekamp, K.E. et al. 1996. Rank and reproduction in female spotted hyenas. Journal of Reproduction and Fertility 108 229–37
Holliday, R. 1989. Food, reproduction and longevity: is the extended lifespan of calorie-restricted animals an evolutionary adaptation? Bioessays 10: 125–7
Holly, J.M.P. et al. 1999. Growth hormone, IGF-1 and cancer. Less intervention to avoid cancer? More intervention to prevent cancer? Journal of Endocrinology 162: 321–30
Horan, G.S. et al. 1994. Homeotic transformation of cervical vertebrae in Hoxa-4 mutant mice. Proceedings of the National Academy of Sciences, USA. 91: 12644–8
Horan, G.S. et al. 1995a. Compound mutants for the paralogous Hoxa-4, Hoxb-4, and Hoxc-4 genes show more complete homeotic transformations and a dose dependent increase in the number of vertebrae transformed. Genes and Development 9: 1667–77
Horan, G.S. et al. 1995b. Mutations in paralogous Hox genes result in overlapping homeotic transformations of the axial skeleton – evidence for unique and redundant function. Developmental Biology 169: 359–72
Houssay, F. 1937. De la nature, des causes, des differences des monstres. Editions Hippocrates, Paris
Hu, D. and J.A. Helms. 1999. The role of sonic hedgehog in normal and abnormal craniofacial morphogenesis. Development 126: 4873–84
Huelsken, J. et al. 2001. Beta-catenin controls hair follicle morphogenesis and stem cell differentiation in the skin. Cell 105: 533–45
Hummel, K.P. 1958. The inheritance and expression of Disorganization, an unusual mutation in the mouse. Journal of Experimental Zoology 137:389–423
Hummel, K.P. 1959. Developmental anomalies in mice resulting from action of the gene Disorganization, a semi-dominant lethal. Pediatrics 23: 212–21
Ianakiev, P. et al. 2000. Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene. American Journal of Human Genetics 68: 38–45
Imperato-McGinley, J. et al. 1974. Steroid 5-alpha-reductase deficiency in man: an inherited form of male pseudohermaphroditism. Science 186: 1213–15
Imperato-McGinley, J. et al. 1991. A cluster of male pseudohermaphrodites with 5-Alpha-reductase deficiency in Papua New Guinea. Clinical Endocrinology 34: 293–8
Incardona, J.P. 1998. The teratogenic Veratrum alkaloid cyclopamine inhibits sonic hedgehog signal transduction. Development 125: 3553–62
International Sequencing Consortium. 2001. Initial sequencing and analysis of the human genome. Nature 409: 860–921
Irving, J. 1862. The drowned women of Wigton, a romance of the Covenant. Porteous and Hislop, Glasgow
Isaac, A. et al. 2000. FGF and genes encoding transcription factors in early limb specification. Mechanisms of Development 93: 41–8
Iwai, T. 1907. A statistical study on the polymastia of the Japanese. Lancet 2: 753–4
Jackson, I.J. 1997. Homologous pigmentation mutations in human, mouse and other model organisms. Human Molecular Genetics 6: 1613–24
Jackson, W.P.U. 951. Osteo-dental dysplasia (Cleidocranial dysostosis) ‘The Arnold Head’. Acta Medica Scandinavica 139: 293–5
Janin, J. 1829. (1998) Une femme à deux têtes. S. Pestel (ed.) La collection électronique de la Bibliotéque Municipale de Lisieux. http://ourworld.compuserve.com./homepages/bibhhlisieux/
Jarvik, G.P. et al. 1994. Non-mendelian transmission in a human developmental disorder: Split Hand/Split Foot. American Journal of Human Genetics 55: 710–13
Jeannotte, L. et al. (1993) Specification of axial identity in the mouse: role of the Hoxa5 (Hox1. 3) gene. Genes and Development 7: 2085–96
Jenkins, P. 1998. Cancer in acromegaly. Trends in Endocrinology and Metabolism 9: 360–6
Johanson, D. and B. Edgar. 1996. From Lucy to language. Orion, London
Joseph, R. and P. Godson. 1988. Peace at last for tragic Rita: white outcase in black skin. Sunday Times (Johannesburg). 28 August. p. 12
Jost, A. 1946–47. Recherches sur la différenciation sexuelle de l’embryon de lapin (Trbisiéme Partie). Archives d’anatomie microscopique et de morphologie expérimental 36: 271–315
Jung, H.-S. et al. 1998. Local inhibitory action of BMPs and their relationships with activators in feather formation: implications for periodic patterning. Developmental Biology 196: 11–23
Kappler, C. 1980. Monstres, démons et merveilles á la fin du Moyen age. Payot, Paris
Kaufman, M.H. and K.S. O’Shea. 1978. Induction of monozygotic twinning in the mouse. Nature 276: 707–8
Keith, A. 1911. An inquiry into the nature of the skeletal changes in acromegaly Lancet i: 993–1002
Kenyon, C. et al. 1993. A C. elegans mutant that lives twice as long as wild type. Nature 366: 461–4
Kere, J. et al. 1996. X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by a mutation in a novel transmembrane protein. Nature Genetics 13: 409–16
Kingdon-Ward, F. 1924. From China to Hkamti Long. Edward Arnold, London
Kingdon-Ward, F. 1937. Plant hunter’s paradise. Jonathan Cape, London
Kirk, G.S. 1974. The nature of the Greek myths. Penguin, Harmondsworth, UK
Knussmann, R. et al. 1992. Relations between sex hormone level and characteristics of hair and skin in healthy young men. American Journal of Physical Anthropology 88: 59–67
Kobelt, G.L. 1844. The female sex organs in humans and some mammals (trans. H.F. Bernays) in Lowry, T.P. (1978) The classic clitoris, historical contributions to scientific sexuality. Nelson-Hall, Chicago
Kohn, M. 1995. The race gallery: the return of racial science. Jonathan Cape, London
Kollar, E.J. and C. Fisher. 1980. Tooth induction in chick epithelium: expression of quiescent genes for enamel synthesis. Science 207: 993–5
Komori et al. 1997. Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts. Cell 89: 755–64
Kondo, S. et al. 2001. The medaka rs-3 locus required for scale development encodes ectodysplasin-A receptor. Current Biology 7: 1201–6
Kondo, T. et al. 1997. Of fingers, toes, and penises. Nature 390: 29
Koren, Y. and E. Negev. 2003. Im Herzen waren wir Riesen. Econ, Munich
Kornak, U. et al. 2000. Mutations in the a3 subunit of the vacuolar H+-ATPase cause infantile malignant osteopetrosis. Human Molecular Genetics 9: 2059–63
Kostic, D. and M.R. Capecchi. 1994. Targeted disruptions of the murine HoxA-4 and HoxA-6 genes result in homeotic transformations of components of the vertebral column. Mechanisms of Development 46: 231–47
Kremer, H. et al. 1995. Male pseudohermaphroditism due to a homozygous missense mutation of the luteinising hormone receptor gene. Nature Genetics 9: 160–4
Krude, H. et al. 1998. Severe early onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans. Nature Genetics 19: 155–7
Kruglyak, L. and D.A. Nickerson. 2001. Variation is the spice of life. Nature Genetics 27: 234–6
Krzisnik, C. et al. 1999. The ‘Little People’ of the Island of Krk – Revisited. Etiology of hypopituitarism revealed. Journal of Endocrine Genetics 1:9–19
Kuester and Happle. 1984. The inheritance of common baldness. Two B or not two B? Journal of the American Academy of Dermatology 11: 921–6
Läära, E. and P. Rantakallio. 1996. Body size and mortality in women: a 29-year follow up of 12,000 pregnant women in northern Finland. Journal of Epidemiology and Community Health 50: 408–14
Lahr, M.M. 1996. The evolution of modern human diversity: a study in cranial variation. Cambridge University Press
Lamb, T.M. et al. 1993. Neural induction by the secreted polypeptide noggin. Science 262: 713–18
Lammer, E.J. et al. 1985. Retinoic acid embryopathy. New England Journal of Medicine 313: 837–41
Landucci, L. 1542, 1927. A Florentine diary from 1450 to 1516 by Luca Landucci, continued by an anonymous writer till 1542 with notes by Iodoco del Badia (trans. A. de Rosen Jervis). J.M. Dent & Sons, London
Lanza, R.P. et al. 2000. Extension of cell life-span and telomere length in animals cloned from senescent somatic cells. Science 288: 665–8
Laqueur, T.W. 1989. ‘Amor Veneris, vel Dulcedo Appeleteur’ pp.90–131 in M. Feher (ed.) Zone 5. Fragments for a history of the human body, part 3. Zone, N.Y.
Laqueur, T.W. 1990. Making sex, body and gender from the Greeks to Freud, Harvard University Press, Cambridge. Mass.
Laue, L.L. et al. 1996. Compound heterozygous mutations of the luteinising hormone receptor gene in Leydig cell hypoplasia. Molecular Endocrinology 10: 987–97
Lawrence, P. 1992. The making of a fly. Blackwell. London
Laycock, J. and P. Wise. 1996. Essential Endocrinology. (3rd ed.) Oxford University Press
Lazner, F. et al. 1999. Osteopetrosis and osteoporosis: two sides of the same coin. Human Molecular Genetics 8: 1839–46
Le Guyader, H. 1998. Étienne Geojfroy Saint-Hilaire (1772–1844): un naturalist visionnaire. Belin, Paris
Le Mouellic, H. et al. 1992. Homeosis in the mouse induced by a null mutation in the Hox-3. 1 gene. Cell 69: 251–64
Le Roith, D. et al. 2001. What is the role of circulating IGF? Trends in Endocrinology and Metabolism 12: 48–52
Lee, C-K. et al. 1999. Gene expression profile of aging and its retardation by caloric restriction. Science 285: 1390–3
Lee, H.W. et al. 1998. Essential role of mouse telomerase in highly proliferative organs. Nature 392: 569–74
Lee, P.A. and S.F. Witchel. 1997. The influence of estrogen on growth. Current opinion in pediatrics 9: 431–6
Lenz, W. 1962. Thalidomide and congenital abnormalities. Lancet i: 45
Leroi, A.M. 2001. Molecular signals versus the loi de balancement. Trends in Ecology and Evolution. 16: 24–9
Leroi, A.M. et al. 2003. Cancer selection. Nature Cancer Reviews 3: 226–31
Lettice, L.A. et al. 2002. Disruption of a long-range cis-acting regulator for Shh causes preaxial Polydactyly. Proceedings of the National Academy of Sciences, USA 99: 7548–53
Levin, M. et al. 1995. A molecular pathway determining left-right asymmetry in chick embryogenesis. Cell 82: 803–14
Levin, M. et al. 1996. Laterality defects in conjoined twins. Nature 384: 321
Lewandoski, M. et al. 2000. Fgf8 signalling from the AER is essential for normal limb development. Nature Genetics 26: 460–3
Lewis, E. 1978. A gene complex controlling segmentation in Drosophila. Nature 27: 565–70
Lewis, T. and D. Embleton. 1908. Split-hand and split-foot deformities, their types, origin, and transmission. Biometrika 6: 26–58
Li, J. et al. 1997. Dinucleotide repeat in the 3’ flanking region provides a clue to the molecular evolution of the Duffy gene. Human Genetics 99: 573–7
Liceti, F. 1634. De monstrorum natura caussis et differentiis. Padua
Licht, P. et al. 1992. Hormonal correlates of ‘masculinisation’ in female spotted hyenas (Crocuta crocuta). 2. Maternal and fetal steroids. Journal of reproduction and fertility 95: 463–74
Lickert, H. et al. 2002. Formation of multiple hearts in mice following deletion of beta-catenin in the embryonic endoderm. Developmental Cell 3: 171–81
Lifton, R.J. 1986. The Nazi doctors: medical kjlling and the pychology of genocide. Macmillan, London
Lindroth, S. 1983. The two faces of Linnaeus, in T. Frangsmyr (ed.) Linnaeus: the man and his work. University of California Press, Berkeley
Linnaeus, C. 1758, 1939. Systema naturae 10th edition. British Museum, London
Linnaeus, C. 1761. Fauna svecica. Stockholm
Lloyd, A.T. 1986. Pussy Cat, Pussy Cat, where have you been? Natural History 95(7): 46–52
Logroño, R. et al. 1997. Heteropagus conjoined twins due to fusion of two embryos: report and review. American Journal of Medical Genetics 73: 239–43
Lopez-Bermejo, A. et al. (2000). Genetic defects of the growth hormone-insulin-like growth factor axis. Trends in Endocrinology and Metabolism 11:39–49
Lufkin, T. et al. 1991. Disruption of the Hox-1. 6 (Hoxa1) homeobox gene results in defects in a region corresponding to its rostral domain of expression. Cell 66: 1105–19
Lupu, F. et al. 2001. Roles of growth hormone and insulin-like growth factor 1 in mouse postnatal growth. Developmental Biology 229: 141–62
McBride, W.B. 1961. Thalidomide and congenital abnormalities Lancet ii: 1358
McEwan, C. et al. 1997. (eds) Patagonia: natural history, prehistory and ethnography at the uttermost ends of the earth. British Museum, London
Mackenbach, J.P. 1991. Narrowing inequalities in children’s height. Lancet 338: 764
McLachlan, J. 1994. Medical embryology. Addison-Wesley, Wokingham
McLaren, A. 1990. What makes a man a man? Nature 346: 216–17
McMahon, J.A. et al. 1998. Noggin-mediated antatonism of BMP signalling is required for growth and patterning of the neural tube and somite. Genes and Development 12: 1438–52
McMullen, G. and K. Pearson. 1913. On the inheritance of the deformity known as split-foot or lobster-claw. Biometrika 9: 381–90
McPherron, A.C. and SJ. Lee. 1997. Doubling muscle in cattle due to mutations in the myostatin gene. Proceedings of the National Academy of Sciences, USA 94: 12457–61
McPherron, A.C. et al. 1997. Regulation of skeletal muscle mass in mice by a new TGF-Beta superfamily member. Nature 387: 83–90
Maden, M. 1999. Heads or tails? Retinoic acid will decide. Bioessays 21: 809–12
Maeder, T. 1998. A few hundred people turned to bone. The Atlantic, February, (two parts)
Manoiloff, E.O. 1931. A rare case of hereditary hexadactylism. American Journal of Physical Anthropology 15: 503–8
Manouvrier-Hanu S. et al. 1999. Genetics of limb anomalies in humans. Trends in Genetics 15: 409–17
Mansholt, U.J. 1987. The increase in the height of Dutchmen and the attraction of tennis. Nederlands Tijdschrift voor Geneeskunde 131: 376
Mark, M. et al. 1993. Two rhombomeres are altered in Hoxa-1 mutant mice. Development 119: 319–38
Maroteaux, P. 1995. Toulouse-Lautrec’s diagnosis. Nature Genetics 11: 362
Maroteaux, P. and M. Lamy. 1965. The malady of Toulouse Lautrec. JAMA, Journal of the American Medical Association 191: 111–13
Marshall, H.K. and H.I. Harder. 1958. Testicular feminising syndrome in male pseudohermaphrodite: report of two cases in identical twins. Obstetrics and Gynecology 12: 284–93
Martin, E. 1880. Histoire des monstres. C. Reinwald, Paris
Martin, G. and J. Oshima. 2000. Lessons from human progeroid syndromes. Nature 408: 263–6
Martinez-Frias, M.-L. 1993. Another way to interpret the description of the Monster of Ravenna of the sixteenth century. American Journal of Medical Genetics 49: 362
Mascie-Taylor, C.G.N and J.L. Boldsen. 1985. Regional and social analysis of height variation in a contemporary British sample. Annals of Human Biology 12: 315–24
Mathon, N.F. et al. 2001. Lack of replicative sensecence in normal rodent glia. Science 291: 872–5
Mayor, A. 2000. The first fossil hunters. Princeton University Press, Princeton, N.J.
Medawar, P.B. 1952. An unsolved problem in biology. H. K. Lewis. London
Melanchthon, P. and M. Luther. 1523 (1823). Interpretation of two horrible monsters [Deuttung der czwo grewlichï Figuren, etc.]
Merimee, T.J. et al. 1981. Dwarfism in the pygmy. New England Journal of Medicine 305: 965–8
Merimee, T.J. et al. 1987. Insulin-like growth factors in pygmies: the role of puberty in determining final stature. New England Journal of Medicine 316: 906–11
Merke, F. 1993. History and iconography of endemic goitre and cretinism. MTP Press, Lancaster
Merlo, G.R. et al. 2002. Mouse model of split hand/foot malformation type 1. Genesis 33: 97–101
Meyers, E.N. and G.R. Martin. 1999. Differences in left-right axis pathways in mouse and chick: functions of FGF8 and SHH. Science 285: 403–6
Miller, R. and S. Austad. 1999. Large animals in the fast lane. Science 285:199
Mills, A.A. et al. 1999. P63 is a P53 homologue required for limb and epidermal morphogenesis. Nature 398: 708–13
Mittwoch, U. 1973. Genetics of sex differentiation. Academic Press, N.Y.
Monreal, A.W. 1999. Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia. Nature Genetics 22: 366–9
Montaigne, M. de. 1580 (1958). Essays (trans. J.M. Cohen). Penguin Books, Harmondsworth, UK
Montaigne, M. de. 1603 (1998). Florio’s translation of Montaigne’s essays. B. R. Schneider (ed.), Renascence Editions, University of Oregon
Moon, A.M. and M.R. Capecchi. 2000. Fgf8 is required for outgrowth and patterning of the limbs. Nature Genetics 26: 455–9
Morin, A. 1996. La teratologic de Geoffroy Saint-Hilaire á nos jours. Bulletin de l’Association des Anatomistes 80: 17–31
Morishima, A. et al. 1995. Aromatase deficiency in male and female siblings caused by a novel mutation and the physiological role of estrogens. Journal of clinical endocrinology and metabolism 80: 3689–98
Mortlock, D.P. and J.W. Innis. 1997. Mutation of Hox a-13 in hand-foot-genital syndrome. Nature Genetics 15: 179–80
Mortlock, D.P. et al. 1996. The molecular basis of hypodactyly (Hd): a deletion in Hox a-13 leads to arrest of digital arch formation. Nature Genetics 13: 284–8
Moskovitz, E. 1987. By the grace of the devil. Rotem, Ramat-Gan, Israel
Muenke M. and PA. Beachy 2000. Genetics of ventral forebrain development and holoprosencephaly. Current Opinion in Genetics and Development 10: 262–9
Mundlos, S. 1999. Cleidocranial dysplasia: clinical and molecular genetics. Journal of Medical Genetics 36: 177–82
Mundlos, S. et al. 1997. Mutations involving the transcription factor CBFAi cause cleiodocranial dysplasia. Cell 89: 773–9
Muragaki, Y. et al. 1996. Altered growth and branching patters in synpoly-dactyly caused by mutations in Hox d-13. Science 272: 548–51
Mya-Tu, M. et al. 1962. Tarong pygmies in North Burma. Nature 195: 131–2
Mya-Tu, M. et al. 1966. The Tarons in Burma. Burma Medical Research Institute, Rangoon. Special Report Series No. 1
Nanni, L. et al. 1999. The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly. Human Molecular Genetics 8: 2479–88
Nanni, L.et al. 2001. SHH mutation is associated with solitary median maxillary central incisor: a study of 13 patients and review of the literature. Journal of Medical Genetics 102: 1–10, 2001
Naski, M.C. et al. 1996. Graded activation of fibroblast growth factor receptor 3 by mutaitons causing achondroplasia and thanatophoric dysplasia. Nature Genetics 13: 233–7
Naski, M.C. et al. 1998. Repression of hedgehog signalling and BMP4 expression in growth plate cartilage by fibroblast growth factor receptor 3. Development 125: 4977–88
Naudin ten Gate L., C. Vermeij-Keers, D.A. Smit, T.W. Cohen-Overbeek, K.B. Gerssen-Schoorl, T. Dijkhuisen. 1995. Intracranial teratoma with multiple fetuses. Pre- and post-natal appearance. Human Pathology 26: 804–7
Neaves, W.B. et al. 1980. Sexual dimorphism of the phallus in spotted hyena (Crocuta crocuta). Journal of Reproduction and Fertility 59: 509–13
Needham, J. 1959. A history of embryology. Cambridge University Press, Cambridge, UK
Netter, A. et al. 1958. Le testicule feminisant. Annates d’ endocrinologie 9: 994–1014
Neubert, R. et al. 1999. Developmental model for thalidomide action. Nature 400: 419–20
Newbery, H.J. and CM. Abbott. 2002. Of mice, men and motor neurons. Trends in Molecular Medicine 8: 88–92
Niccoli, O. 1990. People and prophecy in renaissance Italy, (trans. L. G. Cochrane.) Princeton University Press, Princeton
Niswander, L. et al. 1993. FGF-4 replaces the apical ectodermal ridge and directs outgrowth and patterning of the limb. Cell 75: 579–87
Nonaka, S. et al. 1998. Randomisation of left–right asymmetry due to loss of nodal cilia generating leftward flow of extraembryonic fluid in mice lacking KIF3B motor protein. Cell 95: 839–47
Noramly, S. and B.A. Morgan. 1998. BMPs mediate lateral inhibition at successive stages in feather tract development. Development 125: 3775–87
O’Connell, H.E. et al. 1998. Anatomical relationship between urethra and clitoris. Journal of Urology 159: 1892–7
Olbrich, H. et al. 2002. Mutations in DNAH5 cause primary ciliary dyskinesia and randomisation of left–right asymmetry. Nature Genetics 30: 143–4
Olsen, B.R. et al. 2000. Bone development. Annual Reviews of Cell and Developmental Biology 16: 191–220
On-line Mendelian Inheritance in Man. 2000. OMIM™. McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University, Baltimore, MD, and National Center for Biotechnology Information, National Library of Medicine, Bethesda, MD. http://www.ncbi.nlm.nih.gov/omim/
Oosterhout, van C. et al. 2003. Inbreeding depression and genetic load of sexually selected traits: how the guppy lost its spots. Journal of Evolutionary Biology 16: 273–81
Oostra, R.–J. et al. 1998a. Congenital anomalies in the teratological collection of the Museum Vrolik in Amsterdam, the Netherlands. I: syndromes with multiple congenital anomalies. American Journal of Medical Genetics 77: 100–15
Oostra, R.–J. et al. 1998b. Congenital anomalies in the teratological collection of the Museum Vrolik in Amsterdam, the Netherlands. II: Skeletal Dysplasias. American Journal of Medical Genetics 77: 116–34
Oostra, R.–J. et al. 1998c. Congenital anomalies in the teratological collection of the Museum Vrolik in Amsterdam, the Netherlands. Ill: Primary field defects, sequences and other complex anomalies. American Journal of Medical Genetics 80: 46–59
Oostra, R.–J. et al. 1998d. Congenital anomalies in the teratological collection of the Museum Vrolik in Amsterdam, the Netherlands. IV: Closure defects of the neural tube. American Journal of Medical Genetics 80: 60–73
Oostra, R.–J. et al. 1998e. Congenital anomalies in the teratological collection of the Museum Vrolik in Amsterdam, the Netherlands. V: Conjoined and acardiac twins. American Journal of Medical Genetics 80: 74–89
Oro, A.E. and M.P. Scott. 1998. Splitting hairs: dissecting roles of signaling systems in epidermal development. Cell 95: 575–8
Orr, H.T. 2000. A proposed mechanism of ALS fails the test in vivo. Nature Neuroscience 5: 287–8
Ortega-Ortiz, J.G. and B. Villa-Ramirez. 2000. Polydactyly and other features of the manus of the vaquita, Phocoena sinus. Marine Mammal Science 16: 277–86
Paré, A. 1573 (1971). Des monstres. J. Céard (ed.) Droz, Geneva
Paré, A. 1573 (1982). On monsters and marvels (trans. J. L. Pallister) Chicago University Press, Chicago
Park, K. and L. Daston. 1981. Unnatural conceptions: the study of monsters in sixteenth and seventeenth century France and England. Past and Present 92: 20–54
Parkes, T.L. et al. 1998. Extension of Drosophila lifespan by overexpression of human SOD1 in motorneurons. Nature Genetics 19: 171–4
Partridge, L. and D. Gems. 2002. Mechanisms of ageing: public or private? Nature Reviews Genetics 3: 165–75
Patronek, G.J. et al. 1997. Comparative longevity of pet dogs and humans: implications for gerontology research. Journal of Gerontology 52A: B171–8
Pearson, K. et al. 1913. A monograph on albinism in man. 3 V. text; 3 V. plates. Draper’s company research memoirs, Biometric series X. Dulau & Co. London
Pearson, K. 1908. On the inheritance of the deformity known as split-foot or lobster claw. Biometrika 6: 69–79
Pearson, K. 1913. Notes on the Honduras piebald. Biometrika 9: 330–1
Perrett, D.I. et al. 1994. Facial shape and judgements of female attractiveness. Nature 368: 239–42
Perriton, C. et al. 2002. Sonic hedgehog signalling from the urethral epithelium controls external genital development Developmental Biology 247: 26–46
Piccolo, S. et al. 1996. Dorsoventral patterning in Xenopus: inhibition of ventral signals by direct binding of Chordin to BMP-4. Cell 86: 589–98
Pinto-Correa, C. 1997. The ovary of Eve: egg and sperm and preformationism. Chicago University Press, Chicago
Pletcher, S.D. et al. 2002. Genome-wide transcript profiles in aging and calorically restricted Drosophila melanogaster. Current Biology 30: 712–23
Posel, D. 2001. Race as common sense: racial classification in twentieth century South Africa. African Studies Review 44: 87–113
Posner, G. L. and J. Ware. 1986. Mengele: the complete story. Futura, London
Power, C. and S. Matthews. 1997. Origins of health inequalities in a national population sample. Lancet 350: 1584–9
Qu, S. et al. 1998. Mutations in mouse Aristaless-like4 cause Strong’s luxoid Polydactyly. Development. 125: 2711–21
Quance, E. 1977. Alexander Graham Bell, human inheritance, and the eugenics movement. Research Bulletin of the National Historic Parks and Sites Branch, Parks Canada. No. 62
Quigley, C.A. et al. 1992. Complete deletion of the androgen receptor gene: definition of the null phenotype of the androgen insensitivity syndrome and determination of carrier status. Journal of Clinical Endocrinology and Metabolism 74: 932–3
Ramesar, R.S. et al. 1996. Mapping of the gene for cleidocranial dysplasia in the historical Cape Town (Arnold) kindred and evidence for locus homogeneity. Journal of Medical Genetics 33: 511–14
Ramirez-Solis et al. 1993. Hoxb-4 (Hox-2. 6) mutant mice show homeotic transformation of a cerivical rudiment and defects in the closure of the sternal rudiments. Cell 73: 279–94
Rana, B.K. et al. 1999. High polymorphism at the human melanocortin 1 receptor locus. Genetics 151: 1547–57
Rancourt et al. 1995. Genetic interaction between Hoxb-5 and Hoxb-6 is revealed by nonallelic noncomplementation. Genes and Development 9: 108–22
Reaume, A.G. et al. 1996. Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury. Nature Genetics 13: 43–7
Reed, T.E. and J.V. Neel. 1959. Huntington’s chorea in Michigan. American Journal of Human Genetics 11: 107–635
Reeves, R.H. et al. 2001. Too much of a good thing: mechanisms of gene action in Down syndrome. Trends in Genetics 17: 83–241
Reichert, H. and A. Simeone. 2001. Developmental genetic evidence for a monophyletic origin of the bilaterian brain. Philosophical Transactions of the Royal Society B 356: 1533–44
Reynolds, A.J. et al. 1999. Trans-gender induction of hair follicles. Nature 402: 46–7
Ricklefs, R.E. and C.E. Finch. 1995. Ageing: a natural history. Scientific American, N.Y.
Riddle, R.D et al. 1993. Sonic hedgehog mediates the Polarizing Activity of the ZPA. Cell 75: 1401–16
Robbins, L.S. et al. 1993. Pigmentation phenotypes of variant extension locus alleles result from point mutations that alter MSH receptor function. Cell 72: 827–34
Roberts, R.S. 1974. The making of a Rhodesian myth. Rhodesian History 5: 89–91
Robins, A.H. 1991. Biological perspectives on human pigmentation. Cambridge University Press, Cambridge, UK
Rodriguez, J.M. 1870. Descripcion de un monstruo cuadruple, nacido en Durango el ano de 1860. Gaceta Medica de Mexico 5: 33–48
Roessler, E. et al. 1996. Mutations in the human sonic hedgehog gene cause holoprosencephaly. Nature Genetics 14: 357–60
Root, A. 1998. Editorial: does growth hormone have a role in the management of children with nongrowth hormone deficient short stature and intrauterine growth retardation? Journal of Clinical Endocrinology and Metabolism 83: 1067–9
Rose, M.R. 1984. Laboratory evolution of postponed senescence in Drosophila melanogaster. Evolution 38: 1004–10
Rose, M.R. 1991. Evolutionary biology of ageing. Oxford University Press, N.Y.
Rosen, D.R. et al. 1993. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature 362: 59–62
Rosenbaum, S. et al. 1985. A survey of heights and weights of adults in Great Britain Annals of Human Biology 12: 115–27
Rosenbloom, A.L. and J.G. Guevara-Aguirre. 1998. Lessons from the genetics of Laron syndrome. Trends in Endocrinology and Metabolism 9: 276–83
Rosenburg, N.A. et al. 2002. Genetic structure of human populations. Science 298: 2381–5
Rosenfeld, R.G. et al. 1994. Growth hormone (GH) insensitivity due to primary GH deficiency. Endocrine Reviews 15: 369–90
Rousseau, F. et al. 1994. Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia Nature 371: 252–4
Rousseau, F. et al. 1995. Stop codon FGFR3 mutations in thanatophoric dwarfism type 1. Nature Genetics 10: 11–12
Rubinsztein, D.C. 2002. Lessons from animal models of Huntington’s disease. Trends in Genetics 18: 202–9
Rudolph, K.L. et al. 1999. Longevity, stress response, and cancer in aging telomerase-deficient mice. Cell: 96: 701–12
Russell, A.J. et al. 1994. Mutation in the human gene for 3 alpha-hydroxys-teroid dehydrogenase type II leading to male pseudohermaphroditism without salt loss. Journal of Molecular Endocrinology 12: 225–37
Sadler, T.W. 2000. Langman’s medical embryology (8th ed.) Lippincott Williams & Wilkins, Philadelphia
Saegusa, H. et al. 1996. Targeted disruption of Hoxc-4 locus results in axial skeleton homeosis and malformation of the xiphoid process. Developmental Biology 174:55–64
Saint-Ange, M. 1830. Journal hebdomaidaire de médécine 6: 42–9
Sakai, Y. et al. 20001. The retinoic acid-inactivating enzyme CYP26 is essential for establishing an uneven distribution of retinoic acid along the ante-rio-posterior axis within the mouse embryo. Genes and Development 15: 213–25
Samaras, T. and H. Elrick. 1999. Height, body size and longevity. Acta Medica Okayama 53: 149–69
Samaras, T. et al. 1999. Height, health and growth hormone. Acta Paediatrica 88: 602–9
Sandberg, D.E. et al. 1994. Short stature: a psychosocial burden requiring growth hormone therapy? Pediatrics 94: 832–9
Sato, N. et al. 1999. Induction of the hair growth phase in postnatal mice by localized transient expression of sonic hedgehog. Journal of Clinical Investigation 104: 855–64
Saunders, J.W. 1948. The proximo-distal sequence of origin of the parts of the chick wing and the role of the ectoderm. Journal of Experimental Zoology 108: 363–403
Saunders, J.W. and M.T. Gasseling. 1968. Ectodermal-mesenchymal interactions in the origin of limb symmetry. in R. Fleischmajer and R.F. Billingham (eds). Epithelial-Mesenchymal interactions pp.78–97. Williams and Wilkins, Baltimore
Scarry, E. 2000. On beauty and being just. Duckworth, London
Schächter, F. et al. 1994. Genetic associations with human longevity at the APOE and ACE loci. Nature Genetics 6: 29–32
Schatz, F. 1901. Die Griechischen Götter und die Menschlichen Missgeburten. J. F. Bergmann Verlag, Wiesbaden (reprint 1969, Editions Rodopi, Amsterdam)
Schebesta, P. 1952. Die Negrito Asiens 3 vols. Vienna
Schnaas, G. 1974. El Perro Pelon: mito, fantasia y biologia. Gaceta medica de mexico 108: 393–400
Schnitzer, E. 1888. Emin Pasha in central Africa. Schweinfurth, G., Ratzel, F. Felkin, R.W. Hartlauer, G. (eds) Philip and Son. London
Schweinfurth, G. 1878. The heart of Africa (trans. E. E. Frewer). 3rd edition. Sampson Low, Marston, Searle & Rivington, London
Segrave, K. 1996. Baldness, a social history. McFarland & Co. Jefferson, NC, USA
Sémonin, O. et al. 2001. Identification of three novel mutations of the noggin gene in patients with fibrodysplasia ossificans progressiva. American Journal of Medical Genetics 102: 314–17
Serres, E. 1832. Recherches d’anatomie transcendante et pathologique. Théorie des formations et déformations organiques, appliquée á l’anatomie de Ritta-Christina, et de la duplicité monstrueuse. J.B. Balliére, Paris
Seward, G.R. 1992. The Elephant Man. British Dental Association, London
Shriver, M.D. et al. 2003. Skin pigmentation, biogeographical ancestry and admixture mapping Human Genetics 112: 387–99
Sgrò, C. and L. Partridge. 1999. A delayed wave of death from reproduction in Drosophila. Science 286: 2521–4
Sharpe, P. 2001. Fish scale development: hair today, teeth and scales yesterday? Current Biology 11:R751–2
Sharpe, R.M. 1998. The roles of estrogen in the male. Trends in Endocrinology and Metabolism 9: 371–7
Shay, J.W. and W.E. Wright. 2000. Hayflick, his limit, and cellular ageing. Nature Reviews Molecular Cell Biology 1: 72–5
Shea, B.T and A.M. Gomez. 1988. Tooth scaling and evolutionary dwarfism: an investigation of allometry in human pygmies. American Journal of Physical Anthropology 77: 117–32
Shea, B.T. 1989. Heterochrony in human evolution: the case for neoteny reconsidered. Yearbook of Physical Anthropology 32: 69–101
Shea, B.T. and R.C. Bailey. 1986. Allometry and adaptation of body proportions and stature in African pygmies. American Journal of Physical Anthropology 100: 311–40
Shiels, P.G. et al. 1999. Analysis of telomere lengths in cloned sheep. Nature 399: 317
Shozu, M. et al. 1991. A new cause of female pseudohermaphroditism: placental aromatase deficiency. Journal of Clinical Endocrinology and Metabolism 72: 560–6
Shubin, N.H. and P. Alberch. 1986. A morphogenetic approach to the organization of the tetrapod limb. Evolutionary Biology 20: 319–87
Shubin, N.H. et al. 1997. Fossils, genes and the evolution of animal limbs. Nature 388: 639–48
Sidow, A. et al. 1999. A novel member of the F-box/WD40 gene family, encoding dactylin, is disrupted in the mouse dactylaplasia mutant. Nature Genetics 23: 104–7
Siebold, von C.T. 1878. Die Haarige familie von Ambras. Archiv für Anthropolgie 10: 253–60
Silventoinen, K. et al. 1999. Social background, adult body-height and health. International Journal of Epidemiology 28: 911–18
Siminoski, K. and J. Bain. 1993. The relationship among height, penile length and foot size. Annals of Sex Research 6: 231–5
Sinclair, A.H. et al. 1990. A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif. Nature 346: 240–4
Slijper, E.J. 1942. Biologic-anatomical investigations on the bipedal gait and upright posture in mammals, with special reference to a little goat, born without forelegs. I., II. Proceedings Koninklijke Nederlandse Academie van Wetenschap 45: 288–95; 407–15
Smith, E.P. et al. 1994. Estrogen resistance caused by a mutation in the estrogen-receptor gene in a man. New England Journal of Medicine 331: 1056–61
Smith, R. et al. 1998. Melanocortin 1 receptor variants in an Irish population. Journal of Investigative Dermatology 111: 119–22
Sordino, P. et al. 1995. Hox gene expression in teleost fins and the origin of vertebrate digits. Nature 375: 678–81
Sornson, M.W. et al. 1996. Pituitary lineage determination by the Prophet of Pit-1 homeodomain factor defective in Ames dwarfism. Nature. 384: 327–32
Sparks, C.S. and R.L. Jantz. 2002. A reassessment of human cranial plasticity: Boas revisited. Proceeding of the National Academy of Sciences USA 99: 14636–9
Spemann, H. and H. Mangold 1924. Über die induktion von Embryonalanlagen durch Implantation artfremder Organisatoren. Archiv für miikroskopische Anatomie und Entwicklungsmechanik 100: 599–638
Spencer, R. 2000a. Theoretical and analytical embryology of conjoined twins: Part 1: Embryogenesis. Clinical Anatomy 13: 36–53
Spencer, R. 2000b. Theoretical and analytical embryology of conjoined twins: Part 2: Adjustments to union. Clinical Anatomy 13: 97–20
Spencer, R. 2001. Theoretical and analytical embryology of conjoined twins: Part 3: External, internal (fetuses in fetu and teratomas), and detached (Acardiacs). Clinical Anatomy 14: 428–44
Steinman, G. 2001a. Mechanisms of twinning. I. Effect of environmental diversity on genetic expression in monozygotic multifetal pregnancies. The Journal of Reproductive Medicine 46: 467–72
Steinman, G. 2001b. Laterality and intercellular bonding in monozygotic twinning. The Journal of Reproductive Medicine. 46: 473–9
Stephens, J.C. et al. 2001. Haplotype variation and linkage disequilibrium in 313 human genes. Science 293: 489–93
Stephens, T.D. et al. 2000. Mechanism of action in thalidomide teratogenesis. Biochemical Pharmacology 59: 1489–99
Stevens, G. et al. 1997. Oculocutaneous albinism (OCA2) in sub-Saharan Africa: distribution of the common 2.7-kb P gene deletion mutation. Human Genetics 99: 523–7
Stratakis, C.A. et al. 1998. The aromatase excess syndrome is associated with feminization of both sexes and autosomal dominant transmission of aberrant P450 aromatase gene transcription. Journal of Clinical Endocrinology and Metabolism 83: 1348–57
Sturm, R.A. et al. 1998. Human pigmentation genetics: the difference is only skin deep. Trends in Genetics 20: 712–21
Subramaniam, J.R. et al. 2002. Mutant SOD1 causes motor neuron disease independent of copper chaperone-mediated copper loading. Nature Neuroscience 5: 301–7
Sun, X. et al. 2002. Functions of FGF signalling from the apical ectodermal ridge in limb development. Nature 418: 501–8
Sutton, J.B. 1890. Evolution and disease. Walter Scott, London
Szabo, G. et al. 1969. Racial differences in the fate of the melanosomes. Nature 222: 1081–2
Tabin, C. 1998. A developmental model for thalidomide defects. Nature 396: 322–3
Tabin, C. 1999. Developmental model for thalidomide action – reply. Nature 400: 420
Takahashi, E. Secular trend in milk consumption and growth in Japan. Human Biology 56: 427–37
Ta-Mei, W. et al. 1982. Craniopagus parasiticus: a case report of a parasitic head protruding from the right side of the face. British Journal of Plastic Surgery 35: 304–11
Tang, D.G. et al. 2001. Lack of replicative senesence in cultured rat oligodendrocyte precusor cells. Science 291: 868–71
Tanner, J.M. 1981. A history of the study of human growth. Cambridge University Press, Cambridge, UK
Tanner, J.M. 1984. Foetus into man. (Revised ed.) Harvard University Press, Cambridge, Mass.
Tassabehji, M. et al. 1992. Waardenburg’s syndrome patients have mutations in the human homologue of the Pax-3 paired box gene. Nature 355:635–6
Tatsumi, K. et al. 1992. Cretinism with combined hormone deficiency caused by a mutation in the pit-1 gene. Nature Genetics 1: 56–8
Taussig, H.B. 1988. Evolutionary origin of cardiac malformations. Journal of the American College of Cardiology 12: 1079–86
Tavormina, PL. et al. 1995. Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3. Nature Genetics 9: 321–8
Thadini, K.I. 1934. The toothless men of Sind. Journal of Heredity 26: 65–6
Thangaraj, K. 2003. Genetic affinities of the Andaman Islanders, a vanishing human populations. Current Biology 13: 86–93
Thiery, M. and H. Houtzager. 1997. Der Vrouwen Vrouwlijcheit. Erasmus, Rotterdam
Thompson, A.A. and L.T Nguyen. 2000. Amegakaryocytic thrombocytopenia and radio-ulnar synostosis are associated with HOXA11 mutation. Nature Genetics 26: 397–8
Thompson, C.J.S. 1930 (1994) The history and lore of freaks. Senate. London
Thornhill, R. and S.W. Gangestad 1999. Facial attractiveness. Trends in Cognitive Science 3: 452–60
Tibbies, J.A.R. and M.M. Cohen. 1986. The Proteus syndrome: the Elephant Man diagnosed. British Medical Journal 293: 683–5
Tickle, C. et al. 1975. Positional signalling and specification of digits in chick limb morphogenesis. Nature 20: 199–202
Tietze-Conrat, E. 1957. Dwarfs and jesters in art. Phaidon. London
Tjalma, R.A. 1966. Canine bone sarcoma: estimation of relative risk as function of body size. Journal of the National Cancer Intitute. 36: 1137–50
Toda, K. et al. 1972. Racial differences in melanosomes. Nature New Biology 236: 143–5
Ton, C.T. et al. 1991. Positional cloning and characterization of a Paired Box- and Homeobox-containing gene from the Aniridia region. Cell 67: 1059–74
Touchefeu-Meynier, O. 1992. Kyklops, Kyklopes. text pp. 154–9; plates pp.69–75 in Lexicon iconographicum mythologiae classicae: VI: 1 (text); 2 (plates)
Townsend, P. et al. 1992. Inequalities in health. Penguin Books, Harmondsworth, UK
Trotter, M. 1928. Hair growth and shaving. Anatomical Record 37: 373–9
Tsukui, T. et al. 1999. Multiple left-right asymmetry defects in Shh-/-mutant mice unveil a convergence of the Shh and retinoic acid pathways in the control of Lefty-1. Proceedings of the National Academy of Sciences, USA. 96: 11376–81
Twitty, V.C. 1966. Of scientists and salamanders. W. H. Freeman and Co., San Francisco
Twitty, V.C. and J.L. Schwind. 1931. The growth of eyes and limbs transplanted heteroplastically between two species of Amblystoma (sic) Journal of Experimental Zoology 59: 61–86
Tyson, E. 1699 (1966). A philological essay concerning the pygmies of the ancients. B. Windle (ed.). David Nutt, London
Unthan, C.H. 1935. The armless fiddler: a pediscript. George Allen & Unwin, London
Valenzano, M. et al. 1999. Sirenomelia. Pathological features, antenatal ultrasonographic clues, and a review of current embryogenic theories. Human Reproductive Update 5: 82–6
Valverde, P. et al. 1995. Variants of the melanocyte stimulating hormone receptor gene are associated with red hair and fair skin in humans. Nature Genetics 11: 328–30
Vassart, G. 2000. TSH receptor mutations and diseases Ch. 16a. The Thyroid and Its Diseases, http://www.thyroidmanager.org
Vieille-Grosjean, I. et al. 1997. Branchial Hox gene expression and human craniofaciall development. Developmental Biology 183: 4960
Viljoen, D.L. and P. Beighton. 1984. The split-hand and split-foot anomaly in a central African Negro population. American Journal of Medical Genetics 19: 545–52
Viljoen, D.L. and S.H. Kidson. 1990. Mirror-polydactlyly – pathogenesis based on a morphogen gradient theory. American Journal of Medical Genetics 35: 22935
Voss, J.W and M.G. Rosenfeld. 1992. Anterior pituitary development. Cell 70: 527–30
Vrolik, W. 1834. Over den aard en oorsprong der cyclopie. Niewe verhan-delingen der Eerste Klasse van het Koninklijk Nederland Instituut. 5: 25112
Vrolik, W. 1844–49. Tabulae ad illustrandam embryogenesin hominis et mam-malium tarn naturalem quam abnormem. Amsterdam, London
Waaler, H.T 1984. Height, weight and mortality: the Norwegian experience. Acta Medica Scandinavia Supplement 679: 1–56
Walton, M.T. et al. 1993. Of monsters and prodigies: the interpretation of birth defects in the sixteenth century. American Journal of Medical Genetics 47: 7–13
Watanabe, A. et al. 1998. Epistatic relationship between Waardenburg syndrome genes MITF and PAX3. Nature Genetics 18: 283–6
Weber, G. 1995–99. Lonely islands: the Andamanese. The Andaman Association, Switzerland, http://andaman.org
Weinstein, B.S. and D. Ciszek. 2002. The reserve-capacity hypothesis: evolutionary origins and modern implications of the trade-off between tumor-suppression and tissue repair. Experimental Gerontology 37: 615–27
Westendorp, R.G.J. and T.B.L. Kirkwood. 1998. Human longevity and the cost of reproductive success. Nature 396: 743–6
Wilkie, A.O. et al. 1995. Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome. Nature Genetics 9: 165–72
Williams, D. 1996. Deformed discourse. The function of the monstrous in medieval thought. University of Exeter Press
Williams, G.C. 1957. Pleiotropy, natural selection, and the evolution of senesence. Evolution 11: 398–411
Williams, G.R. 1998. Thyroid hormone action on cartilage and bone: interactions with other hormones at the epiphyseal plate and effects on linear growth. Journal of Endocrinology 157:391–403
Williamson, S. and R. Nowak. 1998. The truth about women. New Scientist. 159: 34–5
Willier, B.H. and J.M. Oppenheimer. 1964. Foundations of experimental embryology. Prentice-Hall, N.J.
Wilmoth, J.R. et al. 2000a. Demography of longevity: past, present, and future trends. Experimental Gerontology 35: 1111–29
Wilmoth, J.R. et al. 2000b. Increase of maximum life-span in Sweden, 1861–1999. Science 289: 2366–86
Wilmut, I. 2002. Are there any normal cloned animals? Nature Medicine 8: 215–16
Wilmut, I. et al. 1997. Viable offspring derived from fetal and adult mammalian cells. Nature 385: 810–13
Wilson, D. 1993. Signs and portents: monstrous births from the Middle Ages to the Enlightenment. Routledge, London
Wilson, J.D. and C. Roehrborn. 1999. Long term consequences of castration in men: lessons from the Skoptzy and the Eunchs of the Chinese and Ottoman Courts. Journal of Clinical Endocrinology and Metabolism 84: 4324–31
Winter, R.M. 1996. What’s in a face? Nature Genetics 12: 124–129
Winter, R.M. and D. Donnai. 1989. A possible human homologue for the mouse mutant disorganisation. Journal of Medical Genetics 26: 417–20
Wittkower, R. 1942. Marvels of the East. Journal of the Warburg and Courtauld Institutes 5: 159–97
Wolpert, L. 1971. Positional information and pattern formation. Developmental Biology 6: 183–224
Woolf, CM. and F.C. Dukepoo. 1969. Hopi Indians, inbreeding, and albinism. Science 164: 30–7
Worden, G. 2002. Mutter Museum. Blast Books, N. Y.
Wright, S. 1935. A mutation of the guinea-pig, tending to restore the pen-tadactyl foot when heterozygous, producing a monstrosity when heterozygous. Genetics 20: 84–107
Wu, W. et al. 1998. Mutations in prop-1 cause familial combined pituitary hormone deficiency. Nature Genetics 18: 147–9
Yang, A. et al. 1999. P63 is essential for regenerative proliferation in limb, craniofacial and epithelial development. Nature 398: 714–18
Yang, Y. et al. 1997. Relationship between dose, distance and time in sonic hedgehog mediated regulation of anteroposterior polarity in the chick limb. Development 124: 4393–4404
Yu, C.E. et al. 1989. Positional cloning of the Werner’s syndrome gene. Science 272: 258–62
Yule, H. 1858. A narrative of the mission sent by the Governor-General of India to the court of Ava in 1855. Bell, N.Y.
Zákány, J. et al. 1997. Regulation of number and size of digits by posterior Hox genes: A dose dependent mechanism with potential evolutionary implications. Proceeding of the National Academy of Sciences, USA 94: 1395–13700
Zapperi. R. 1995. Ein Haarmensch auf einem Gamälde von Agostino Carracci. in Hagner, M. (ed.) Der falsche Körper: Bieträge zu einer Geschichte der Monstrositäten. Wallstein, Göttingen
Zekraoui, L. et al. 1997. High frequency of the apolipoprotein 84 allele in African pygmies and most of the African populations in sub-Saharan Africa. Human Biology 69: 575–81
Zeng, X. et al. 2001. A freely diffusible form of sonic hedgehog mediates long-range signalling. Nature 411: 716–20
Zguricas, J. et al. 1999. Clinical and genetics studies on 12 preaxial polydactlyly families and refinement of the localization of the gene responsible to a 1. 9 cM region on chromosome 7q35. Journal of Medical Genetics 36: 32–40
Zhou, X.–P. et al. 2000. Germline and germline mosaic PTEN mutations associated with a Proteus-like syndrome of hemihypertrophy, lower-limb asymmetry, arteriovenous malformations and lipomatosis. Human Molecular Genetics 19: 765–8
Zhou, X.-P. et al. 2001. Association of germline mutation in the PTEN tumor suppressor gene and Proteus and Proteus-like syndromes. Lancet 358:210–11
Zimmerman, L.B. et al. 1996. The Spemann organizer signal noggin binds and inactivates Bone morphogenetic protein-4. Cell 86: 599–606
Zou, H. and L. Niswander. 1996. Requirement for BMP signalling in inter-digital apoptosis and scale formation. Science 272: 738–41