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By Jeffery C. Hall

Advances in Genetics raises its concentrate on glossy 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 put up very important stories of the broadest curiosity to geneticists and their colleagues in affiliated disciplines.

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Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. Arch. Neurol. (Chicago) 18:603-618. , and Lamhert, E. H. (1968b). Lower motor and primary sensory neuron diseases with permeal muscular atrophy. Arch. Neurol. (Chicago) 18:618-625. Dyck, P. , and Carney, J. A. (1993). Hereditary motor and sensory neuropathies. In “Peripheral Neuropathy” (P. J. Dyck, P. K. Thomas, J. W. Griftin, P. A. Low, and J. ), pp. 1094-1 136. Saunders, Philadelphia. , Litchy, W. , Bird, T. , Chance, P.

Genet. 3: 1699-1 700. , and van Broeckhoven, C. (1993). Origin of the de novo duplication in Charcot-Marie-Tooth disease typetA: Unequal non-sister chromatid exchange during spermatogenesis. Hum. Mol. Genet. 2:2031-2035. Patel, P. , and Lupski, J. R. (1994). Charcot-Marie-Tooth disease: A new paradigm for the mechanism of inherited disease. Trends Genet. 10:128-133. Patel, P. , Garcia, C. , Slaugenhaupt, S. , Ledbetter, D. , and Lupski, J. R. (1990). Genetic mapping of autosornal dominant Charcot-Marie-Tooth disease in a large French-Acadian kindred: Identification of new linked markers on chromosome 17.

45:953-958. , Hoogendijk,J. , Barker, D. , Bolhuis, P. ,and the HMSN Collaborative Research Group (1991). Duplication in chromosome 1 7 ~ 1 1 . 2in Charcot-Marie-Tooth neuropathy type la (CMTla). Neuromuscular Disord. 1:93-97. , and the HMSN Collaborative Research Group (1992). 2 duplication in Charcot-Marie-Tooth neuropathy type la (CMT la). Med. Genet. 29:5-11. , Pfeiffer, R. , and van Broeckhoven, C. (1994). Identification of a de nowo insertional mutation in Po in a patient with a Dejerine-Sottas syndrome (DSS) phenotype.

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