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Showing articles 0 to 8 of 8 Filter Applied: RFLPs (Click to remove) Genetic Linkage of Hereditary Motor & SensoryNeuro Type I (Charcot-Marie-Tooth Disease) to Chrom 1 & 17 Neurol 40:1450-1453, Defesche,J.C.,et al, 1990 DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis Hum Genet 82:55-58, Defesche,J.C.,et al, 1989 Unusual Variants of Alexander's Disease Ann Neurol 57:327-338, van der Knaap,M.S., et al, 2005 Diagnosis of McArdle's Disease by Molecular Genetic Analysis of Blood Neurol 47:579-580, El-Schahawi,M.,et al, 1996 Molecular Genetic Heterogeneity of Myophosphorylase Deficiency (McArdle's Disease) NEJM 329:241-245, Tsujino,S.,et al, 1993 Molecular Genetics of Duchenne and Becker Muscular Dystrophy J Pediatr 117:1-15, Darras,B.T., 1990 Hunter Disease (Mucopolysaccharidosis Type II) in a Karyotypically Normal Girl Clin genet 37:355-362, Clarke,J.T.,et al, 1990 A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy NEJM 320:1300-1305, Singh,G.,et al, 1989 Showing articles 0 to 8 of 8