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


By Jeffery C. Hall

Advances in Genetics raises its concentrate on glossy human genetics and its relation to medication with the merger of this long-standing serial with Molecular Genetic drugs . This merger affirms theAcademic Press dedication to post very important experiences of the broadest curiosity to geneticists and their colleagues in affiliated disciplines.

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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. Neurology 42:597601. Lupski, J. , Barker, D. E, Killian, J. , Garcia, C. , and Patel, P. 1. (1991). DNA duplication associated with Charcot-Marie-Tooth disease type 1A. ) 66:219-239. Lupski, J. , Wise, C. , Parke, J. , Glaze, D. , Ledbetter, D.

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). Prevalence of hereditary motor and sensory neuropathy in Cantabria.

15:4488-4498. , Neuberg, D. , and Schachner, M. (1996). Mice deficient in the gene for connexin32 show pathological changes in peripheral nerves. 5th Annu. Eur. , London, 1996. , Lensch, M. , Hanemann, C. , Muller, H. , Bird, T. , and Chance, P. F. (1992). 2associated with Charcot-Marie-Tooth 1A. Nat. Genet. 1:176-179. McAlpine, P. , Hahn. A. , Kaita, H.. , Cox, D. , and Yee, W. C. (1990). Localisation of a locus for Charcot-Marie-Tooth neuropathy type la (CMTlA) to chromosome 17. Genomics 7:408-415.

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