Мутанты. О генетической изменчивости и человеческом теле.

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: 240-244

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. "Uber die induktion von Embryonalanlagen durch Implantation artfremder Organisatoren.Archiv f"ur 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