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Molecular Genetic Advances in Fragile X Syndrome
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Molecular Genetics in Neurology
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Brief Report:Intragenic Deletion of the Kalig-1 Gene in Kallmann's Syndrome
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Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
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Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
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Spinal Muscular Atrophies
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Genetic Linkage of Hereditary Motor & SensoryNeuro Type I (Charcot-Marie-Tooth Disease) to Chrom 1 & 17
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Hunter Disease (Mucopolysaccharidosis Type II) in a Karyotypically Normal Girl
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The Molecular Genetic Revolution, Its Impact on Clinical Neurology
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