Арман Мари Леруа - Мутанты. О генетической изменчивости и человеческом теле.

Schnaas, G.1974. ElPerro Pelon: mito, fantasia уbiologia. Gaceta medica de mexico 108: 393-400

Schnitzer, E.1888. Emin Pasha in central Africa. Schweinfurth, G., Ratzel, F. Felkin, RW. Hartlatier, 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

Semonin, 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: 314-317

Serres, E.1832. Recherches d'anatomie transcendante et pathologique. Théorie des formations et déformations organiques, appliquée à I'anatomie de Ritta-Christina, et de la duplicité monstrueuse. J.B. Balliere, 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: 387-399

Sgro, C.and L. Partridge.1999 . A delayed wave of death from reproduction in Drosophila. Science 286: 2521-2524

Sharpe, P.2001. Fish scale development: hair today, teeth and scales yesterday? Current Biology II: R751-752

Sharpe, R.M.1998. The roles of estrogen in the male. Trends in Endocrinology and Metabolism 9: 371-377

Shay, J.W.and W.E.Wright. 2000. Hayflick, his limit, and cellular ageing. Nature Reviews Molecular Cell Biology I: 72-75

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: 117-132

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: 311-340

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: 560-566.

Shubin, N.H.and P. Alberch.1986. A morphogenetic approach to the organization of the tetrapod limb. Evolutionary Biology 20: 319-387

Shubin, N.H.et al. 1997. Fossils, genes and the evolution of animal limbs. Nature 388: 639-648

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: 104-107

Siebold, von C.T.1878. Die Haarige familie von Ambras. Archiv für Anthropolgie 10: 253-260

Silventoinen, K.et al. 1999. Social background, adult body-height and health. International Journal of Epidemiology 28: 911-918

Siminoski, K.and J. Bain.1993. The relationship among height; penile length and foot size. Annals of Sex Research 6: 231-235

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. 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