Clinical Genetics in Neurological Disease
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Molecular Genetics in Neurology
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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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Alexander Disease, Ventricular Garlands and Abnormalities of the Medulla and Spinal Cord
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Linkage of Proximal Myotonic Myopathy to Chromosome 3q
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Hereditary Spastic Paraplegia:Advances in Genetic Research
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Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
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Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
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Detecting Susceptibility to Malignant Hyperthermia
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Brief Report:Intragenic Deletion of the Kalig-1 Gene in Kallmann's Syndrome
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Molecular Genetics of Duchenne and Becker Muscular Dystrophy
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Hunter Disease (Mucopolysaccharidosis Type II) in a Karyotypically Normal Girl
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Retinitis Pigmentosa
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