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By Jeffery C. Hall

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

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J. 62:172-182. Davies, D. M. ( 1954). Recurrent peripheral nerve palsies in a family. Lancet 2:266-268. 38 C. Bell and N. Hailes Dehruyne, J.. , and Martin, J . J. (1980). Hereditary pressure sensitive neuropathy. J. Neurol. Sci. 47:385-394. Defesche. 1. , Hoogendijk, J. , Ongerhoer de Visser, B. , and Bolhuis, P. A. ( 1990). Genetic linkage of hereditary motor and sensory neuropathy type 1 (Charcot-Marie-Tooth disease) to markers of chromosomes 1 and 17. Neurologj 40:1450-1453. , and Sottas, J.

And van Broeckhoven, C . (1994a). Linkage and mutation analysis in an extended family with Charcot-Marie-Tooth neuropathy type 1B. J. Med. Genet. 3:811-815. , and van Broeckhoven, C. Identification of a 5’ splice site mutation in the PMP-22 gene in autosoinal dominant Charcot-Marie-Tooth disease type 1. Hum. Mol. Genet. 3;:515-516. , Brice, A,, Mostacciuolo, M. , Savontaus, M. , Mariman, E. C. , Gabreels-Festen, A. A. W. , Burgunder, 1. , Hanemann, C. , Muller, H. , Hertz, J. , Schorderet, D. , Gal, A,, and van Broeckhoven, C .

Mol. Genet. 3:29-31. Filhin, M. , Walsh, F. , Trapp, B. , Piney, J. , and Tennekoon, G. I. (1990). Role of myelin Po protein as a homophilic adhesion molecule. Nature (London) 344:871-872. Fischheck, K. , Roses, A. , and Fryns, J. P. (1986). X-linked neuropathy: Gene localisation with DNA probes. Ann. Neurol. 20:527-532. , Wieacker, P. E, Ropers, H. , and Wienker, T. E (1985). X-linked dominant Charcot-Marie-Tooth disease: Suggestion of linkage with a cloned DNA sequence from the proximal Xq. Hum.

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