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Showing articles 0 to 7 of 7 Filter Applied: RFLPs (Click to remove) Unusual Variants of Alexander's Disease Ann Neurol 57:327-338, van der Knaap,M.S., et al, 2005 Prenatal Diagnosis of Wilson's Disease by Analysis of DNA Polymorphism NEJM 327:57, Cossu,P.,et al, 1992 Central Nervous System Lesions in von Hippel-Lindau Syndrome JNNP 55:898-901, Neumann,H.P.H.,et al, 1992 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 Homing in on Wilson's Disease Editorial, Lancet 1:822-8231989., , 1989 A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy NEJM 320:1300-1305, Singh,G.,et al, 1989 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 Showing articles 0 to 7 of 7