Изменить стиль страницы

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: 579-587

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: 839-847

Noramly, S.and B.A. Morgan.1998. BMPs mediate lateral inhibition at successive stages in feather tract development.Development 125: 3775-3787

O'Connell, H.E.et al. 1998. Anatomical relationship between urethra and clitoris.Journal of Urology 159: 1892-1897

Olbrich, H.et al. 2002. Mutations in DNAH5 cause primary ciliary dyskinesia and randomisation of left-right asymmetry.Nature Genetics 30: 143-144

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: 273-281

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: 100-115

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 7 7: 116-134

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. i998d. 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. 19986. 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: 575-578

Orr, H.T.2000. A proposed mechanism of ALS fails the test in vivo.Nature Neuroscience 5: 287-288

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: 277-286

Pare, A.1573 (1971). Des monstres.J. Ceard (ed.) Droz, Geneva

Pare, 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 over expression of human SOD1 in motorneurons.Nature Genetics 19: 171-174

Partridge, L.and D. Gems.2002. Mechanisms of ageing: public or private?Nature Reviews Genetics 3: 165-175

Patronek, G.J.et al. 1997. Comparative longevity of pet dogs and humans: implications for gerontology research.Journal of Gerontology 52A: B171-178

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: 330-331

Perrett, D.I.et al. 1994. Facial shape and judgments of female attractiveness.Nature 368: 239-242

Perriton, C.et al. 2002. Sonic hedgehog signalling from the urethral epithelium controls external genital developmentDevelopmental Biology 247: 26-46

Piccolo, S.et al. 1996. Dorsoventral patterning in Xenopus: inhibition of ventral signals by direct binding of Chord in to BMP-4.Cell 86: 589-598

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: 712-723

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: 1584-1589

Qu, S.et al. 1998. Mutations in mouse Aristaless-like4 cause Strong's luxoid polydactyly.Development. 125: 2711-2721

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: 932-933

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: 511-514

Ramirez-Soliset 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: 279-294

Rana, B.K.et al. 1999. High polymorphism at the human melanocortin 1 receptor locus.Genetics 151: 1547-1557

Rancourtet al. 1995. Genetic interaction between Hoxb-5 and Hoxb-6 is revealed by nonallelic noncomplementation.Genes and Development 9: 108-122

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: 43-47

Reed, Т.Е.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 В 356: 1533-1544

Reynolds, A.J.et al. 1999. Trans-gender induction of hair follicles.Nature 402: 46-47

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: 1401-1416