Книга Мутанты - Арман Мари Леруа

Boardman, J. 1997b. The great god Pan. Thames and Hudson, London

Boas, F. 1912. Changes in bodily form of descendants of immigrants. American Anthropologist 14: 530-562

Bodnar, A.G. et al. 1998. Extension of life-span by introduction of telomerase into normal human cell. Science 279: 349-351

Bogin, B. 1999. Patterns of human growth, 2nd ed. Cambridge University Press, Cambridge. UK

Bonaventure, J. et al. 1996. Common mutations in the Fibroblast Growth Factor Receptor 3 (FGFR3) gene account for achondroplasia, hypochondroplasia and thanatophoric dwarfism. American journal of Medical Genetics 63: 148-154

Bondeson, J. 1997. A cabinet of medical curiosities. Tauris, London

Bondeson, J. 2000. The two-headed boy and other medical marvels. Cornell University Press, Ithaca. N.Y.

Bondeson, J. and A.E.W. Miles. 1996. The hairy family of Burma: a four generation pedigree of congenital hypertrichosis lanuginosa. Journal of the Royal Society of Medicine 89: 403-408

Bornstein, P.E. and R.R. Peterson. 1966. Numerical variation in the presacral vertebral column in three population groups. American Journal of Physical Anthropology 25: 139-146

Boruwlaski, J. 1792. The Memoirs of the celebrated dwarf Joseph Boruwlaski, A Polish gentleman containing a faithful and curious account of his birth, education, marriage, travels and voyages, (trans. S. Freeman) 2nd ed. J. Thompson. Birmingham

Boulet and Capecchi. 1996. Targeted disruption of Hoxc-4 causes esophageal defects and vertebral transformation. Developmental Biology 177: 232-249

Boyd, W.C. 1955. Genetics and the races of man. Little, Brown and Co., Boston

Brandtt A. 1897. Üeberdiesogenannten Hundemenschen, beziehungsweise über Hypertrichosis universalis. Biologische Zentralblatt 17: 161-179

Broberg, G. 1983. Homo sapiens. Linnaeus' classification of man. in T. Frangsmyr, (ed.) Linnaeus: the man and his work. University of California Press, Berkley

Brockes, J.P. 1998. Regeneration and cancer. Biochimica et biophysica acta. 1377 M1-M11

Brown-Borg, H.M. et al. 1996. Dwarf mice and ageing process. Nature 384: 33

Browne, T. 1904. The works of Thomas Browne. C. Sayle (ed.) Grant Richards, London

Brueckner, M. 2001. Cilia propel the embryo in the right direction. American Journal of Medical Genetics 101: 339-344

Brunet, L.J. et al. 1998. Noggin, cartilage morphogenesis, and joint formation in the mammalian skeleton. Science 280: 1455-1457

Brunkow, M.E. et al. 2001. Bone dysplasia sclerosteosis results from loss of the SOST gene product, a novel cystine knot-containing protein. American Journal of Human Genetics 68: 577-589

Bruyn, G.W. and L.N. Went. 1986. Huntington's Chorea, in Vinken, G. W. et al. (eds.) Extrapyramidal disorders: handbook of clinical neurology 49: 267-273

Buffon, G.L. 1777. Histoire naturelle générale et particulière. Imprimerie Royale, Paris

Burn, J. and T. Strachan. 1995. Human embryo use in developmental research. Nature Genetics 11: 3-6

Callahan, C.A. and A.E. Oro. 2001. Monstrous attempts at adnexogenesis: regulating hair follicle progenitors through sonic hedgehog signalling. Current Opinion in Genetics and Development 11: 541-546

Cargill, M. et al. 1999. Characterisation of single-nucleotidepolymorphisms in coding regions of human genes. Nature Genetics 22: 231-238

Carpenter, E.M. et al. 1993. Loss of Hox-Al (Hox-1.6) function results in the reorganisation of the murine hindbrain. Development 118: 1063-1075

Casey, B. and B.P. Hackett. 2000. Left-right axis malformations in man and mouse. Current Opinon in Genetics and Development 10: 257-261

Cavalli-Sforza, L.L. 1986. The African pygmies. Academic Press, N.Y.

Cavelaars, A.E.J.M. et al. 2000. Persistent variations in average height between countries and between socio-economic groups: an overview of 10 European countries Annals of Human Biology 27: 407-421

Celli, J. et at. 1999. Heterozygous germline mutations in the P53 homolog p63 are the cause of EEC syndrome. Cell 99: 143-151

Chapman, T. and L. Partridge. 1996. Female fitness in Drosophila melanogaster: an interaction between the effect of nutrition and of encounter rates with males. Proceedings of the Royal Society, London Series ВBiological Sciences 263: 755-759

Charlesworth, B. 1996. Evolution of senescence: Alzheimer's disease and evolution. Current Biology 6: 20-22

Chen, L. et al. 2001. A Ser{j65)->Cys mutation of fibroblast growth factor receptor 3 in mouse downregulates ihh / PTHrP signals and causes severe achondroplasia. Human Molecular Genetics 10: 457-465.

Chen, Y. et al. 2000. Conservation of early odontogenetic signaling pathways in Aves. Proceedings of the National Academy, USA 97: 10044-10049

Chiang, C. et at. 1996. Cyclopia and defective axial patterning in mice lacking sonic hedgehog gene function. Nature 383: 407-412

Chiang, C. et al. 2001. Manifestation of the limb prepattern: limb development in the absence of sonic hedgehog function. Developmental Biology 236: 421-435

Chisaka, O. and M.R. Capecchi. 1991. Regionally restricted developmental defects resulting from targeted disruption of the mouse homeobox gene hox-1.5 (HoxA3). Nature 350: 473-479

Cibelli, J.B. et at. 2002. The health profile of cloned animals. Nature Biotechnology 20: 13-14

Clark, R.M. et al. 2001. Reciprocal mouse and human limb phenotypes caused by gain and loss-of-function mutations affecting Lmbn. Genetics 159: 715-726

Coates, M.I. and J.A. Clack. 1990. Polydactyly in the earliest tetrapod limbs. Nature 347: 66-69.

Cockayne, E.A. 1933. Inherited abnormalities of the skin and its appendages. Oxford University Press, London

Cohen, M.M. 2002. Bone morphogenetic proteins with some comments on fibrodysplasia ossificans progressiva. American Journal of Medical Genetics 109: 87-92

Cohen, M.M. 1988. Further diagnostic thoughts about the Elephant Man. American Journal of Medical Genetics 29: 777-782