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Showing articles 0 to 2 of 2 Filter Applied: genetic diagnosis,prenatal (Click to remove) Molybdenum Cofactor Deficiency Neurol 85:e175-e178, Nagappa, M.,et al, 2015 Duplication of Part of Chromosome 17 is Commonly Associated with HMSN Type I (Charcot-Marie-Tooth Disease Type 1) Ann Neurol 31:570-572, Hallam,P.J.,et al, 1992 Showing articles 0 to 2 of 2