Download e-book for iPad: Advances in Genetics, Vol. 36 by Jeffery C. Hall

By Jeffery C. Hall

ISBN-10: 012017636X

ISBN-13: 9780120176366

Advances in Genetics raises its specialise in sleek human genetics and its relation to drugs with the merger of this long-standing serial with Molecular Genetic drugs . This merger affirms theAcademic Press dedication to submit very important studies of the broadest curiosity to geneticists and their colleagues in affiliated disciplines.

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Extra info for Advances in Genetics, Vol. 36

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Genet. 5:31-34. , and lonasescu, V. Mutation of the myelin Po gene in CharcotMarie-Tooth neuropathy type 1B. Hum. Mol. Genet. 2:1369-1372. , and Murai, Y. (1993d). Mutation of the myelin Po gene in Charcot-Marie-Tooth neuropathy type 1. Biochem. Biophys. Res. Commun. 194:13171322. , Nicholson, G . , Ouvrier, R. , and Tachi, N. (1993e). De now muration of the myelin Po gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type Ill). Not. Genet. 5:266-268. , and de Recondo, J. (1992).

Mol. Genet. 3:223-228. Charcot, J. , and Marie, I? (1886). Sur une fortne particullere d’Atrophie Musculaire Progressive, souvent Familiale, debutant par les Reds et les Jamhes, et atteignant plus les Mains. Rev. Med. (Paris) 6:97-138. , Fairweather, N. , Mostacciuolo, M. , Monaco, A. ,Fischbeck, K. , and Haites, N. E. (1994). X-linked Charcot-Marie-Tooth disease (CMTX1): A study of 15 families with 12 highly informative polymorphisms. J. Med. Genet. 31:193-196. , Polo, J. , and Berciano, 1. (1987).

King, M. , Anderson, L. , Dazin, P. , Punnett, H. , Schonherg, S. , Shull, M. , Lovelace, R. , and Conneally, P. M. (1991). Chromosome 1 Charcot-Marie-Tooth disease (CMTlB) locus in the Fcy receptor gene region. Hum. Genet. 881-12. , and Axel, R. (1985). Isolation and sequence of a cDNA encoding the major structural protein of peripheral myelin. )40501-508. Loprest, L. , Pericak-Vance, M. , Stajich, 1.. Gaskell, P. , Lucas, A. , Lennon, E, Yamaoka, L. , Roses, A. , and Vance, J. M. (1992). Linkage studies in Charcot-Marie-Tooth disease type 2: Evidence that CMT types 1 and 2 are distinct genetic entities.

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Advances in Genetics, Vol. 36 by Jeffery C. Hall


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