Robbins, L.S.et al. 1993. Pigmentation phenotypes of variant extension locus alleles result from point mutations that alter MSH receptor function.Cell 72: 827-834

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: 357-360

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: 1067-1069

Rose, M.R.1984. Laboratory evolution of postponed senescence in Drosophila melanogaster.Evolution 38: 1004-1010

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: 115-127

Rosenbloom, A.L.and J.G. Guevara-Aguirre.1998. Lessons from the genetics of Laron syndrome.Trends in Endocrinology and Metabolism 9: 27-83

Rosenburg, N.A.et al. 2002. Genetic structure of human populations.Science 298: 2381-2385

Rosenfeld, R.G.et al. 1994. Growth hormone (GH) insensitivity due to primary GH deficiency.Endocrine Reviews 15: 369-390

Rousseau, F.et al. 1994. Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia.Nature 371: 252-254

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: 202-209

Rudolph, K.L.et al. 1999. Longevity, stress response, and cancer in aging telomerase-deficient mice.Cell: 96: 701-712

Russell, A.J.et al. 1994. Mutation in the human gene for 3 alpha-hydroxysteroid dehydrogenase type II leading to male pseudohermaphroditism without salt loss.Journal of Molecular Endocrinology 12: 225-237

Sadler, T.W.2000. Longman'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 6:42-49

Sakai, Y.et al. 2001. The retinoic acid-inactivating enzyme CYP26 is essential for establishing an uneven distribution of retinoic acid along the anterio-posterior axis within the mouse embryo.Genes and Development 15: 213-225

Samaras, T.and H. Elrick.1999. Height, body size and longevity.Acta Medica Okayama 53: 149-169

Silmaras, T.et al. 1999. Height, health and growth hormone.Acta Paediatrica 88: 602-609

Sandberg, D.E.et al. 1994. Short stature: a psychosocial burden requiring growth hormone therapy?Pediatrics 94: 832-839

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: 855-864

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. Fleischmajerand R.F. Billingham(eds). Epithelial-Mesenchymal interactionspp. 78-97 Williams and Wilkins, Baltimore

Scarry, E.2000. On beauty and being just.Duckworth, London

Schachter, F.et al. 1994. Genetic associations with human longevity at the APOE and ACE loci.Nature Genetics 6: 29-32

Schatz, E.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. 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