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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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.