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Showing articles 0 to 12 of 12 Filter Applied: molecular genetics (Click to remove) Molecular Basis of the Neurodegenerative Disorders NEJM 340:1970-1980, Martin,J.B., 1999 Correlations Between Triplet Repeat Expansion and Clinical Features in Huntington's Disease Arch Neurol 113:749-753, Claes,S.,et al, 1995 Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat Ann Neurol 37:769-775, Ikeuchi,T.,et al, 1995 The Prevention of Neurogenetic Disease Arch Neurol 52:356-362, 3451995., Rosenberg,R.N.&Iannaccone,S.T., 1995 The Neurogenetic Genie:Testing for Huntington's Disease Mutation Neurol 44:1369-1373, 1533-15361994., Hersch,S.,et al, 1994 CAG Repeat Size and Clinical Presentation in Huntington's Disease Neurol 44:1137-1143, Ashizawa,T.,et al, 1994 A Worldwide Study of the Huntington's Disease Mutation, The Sensitivity & Specificity of Measuring CAG Repeats NEJM 330:1401-1406, 14501994., Kremer,B.,et al, 1994 Trinucleotide Repeat Length and Rate of Progression of Huntington's Disease Ann Neurol 36:630-635, Illarioshkin,S.N.,et al, 1994 Trinucleotide Repeat Expansion in Neurological Disease Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994 Clinical Consequences of Isolating the Gene for Huntington's Disease BMJ 307:397-398, Harper,P.S., 1993 Molecular Genetics in Neurology Ann Neurol 34:757-773, Martin,J.B., 1993 The Molecular Genetic Revolution, Its Impact on Clinical Neurology Arch Neurol 45:1366-1376, Payne,C.S.&Roses,A.D., 1988 Showing articles 0 to 12 of 12