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![]() 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: 288-295; 407-415 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: 1056-1061 Smith, R. et al. 1998. Melanocortin 1 receptor variants in an Irish population. Journal of Investigative Dermatology III: 119-122 Sordino, P. et al. 1995. Hoxgene expression in teleostfins and the origin of vertebrate digits. Nature 375: 678-681 Sornson, M.W. et al. 1996. Pituitary lineage determination by the Prophet of Pit-1 homeodomain factor defective in Ames dwarfism. Nature. 384: 327-332 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: 14636-14639 Spemann, H. and H. Mangold. 1924. Über die induktion von Embryonalanlagen durch Implantation artfremder Organisatoren. Archiv für mikroskopische 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: 428-444 Steinman, G. 2001a. Mechanisms of twinning. I. Effect of environmental diversity on genetic expression in monozygotic multifetal pregnancies. The Journal of Reproductive Medicine 46: 467-472 Steinman, G. 2001b. Laterality and intercellular bonding in monozygotic twinning. The Journal of Reproductive Medicine 46: 473-479 Stephens, J.C. et al. 2001. Haplotype variation and linkage disequilibrium in 313 human genes. Science 293: 489-493 Stephens, T.D. et al. 2000. Mechanism of action in thalidomide teratogenesis. Biochemical Pharmacology 59: 1489-1499 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: 523-527 Stratakis, C.A. et al. 1998. The aromatase excess syndrome is associated with feminization of both sexes and autosomal dominant transmission of aberrant P 450 aromatase gene transcription. Journal of Clinical Endocrinology and Metabolism 83: 1348-1357 Sturm, R.A. et al. 1998. Human pigmentation genetics: the difference is only skin deep. Trends in Genetics 20: 712-721 Subramaniam, J.R. et al. 2002. Mutant SODI causes motor neuron disease independent of copper chaperone-mediated copper loading. Nature Neuroscience 5: 301-307 Sun, X. et al. 2002. Functions of FGF signalling from the apical ectodermal ridge in limb development. Nature 418: 501-508 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: 1081-1082 Tabin, C. 1998. A developmental model for thalidomide defects. Nature 396: 322-323 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: 427-437 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: 304-311 Tang, D.G. et al. 2001. Lack of replicative senesence in cultured rat oligodendrocyte precusor cells. Science 291: 868-871 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: 635-636 Tatsumi, K. et al. 1992. Cretinism with combined hormone deficiency caused by a mutation in the pit-1 gene. Nature Genetics 1: 56-58 Taussig, H.B. 1988. Evolutionary origin of cardiac malformations. Journal of the American College of Cardiology 12: 1079-1086 Tavormina, P.L. et al. 1995. Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3. Nature Genetics 9: 321-328 Thadini, K.I. 1934. The toothless men of Sind. Journal of Heredity 26: 65-66 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: 397-398 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: 452-460 Tibbies, J.A.R and M.M. Cohen. 1986. The Proteus syndrome: the Elephant Man diagnosed. British Medical Journal 293: 683-685 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 Institute. 36: 1137-1150 Toda, K. et al. 1972. Racial differences in melanosomes. Nature New Biology 236: 143-145 Ton, C.T. et al. 1991. Positional cloning and characterization of a Paired Box- and Homeobox-containing gene from the Aniridia region. 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