Unusual Variants of Alexander's Disease
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Linkage of Proximal Myotonic Myopathy to Chromosome 3q
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Misdiagnosis Revealed by Genetic Linkage Analysis in a Family with Wilson Disease
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Mapping of Hereditary Neuralgic Amyotrophy (Familial Brachial Plexus Neuropathy) to Distal Chromosome 17q
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Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
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Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus
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The Neurogenetic Genie:Testing for Huntington's Disease Mutation
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DNA Analysis in Finnish Patients with Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)
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Direct Diagnosis of Myotonic Dystrophy with a Disease-Specific DNA Marker
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Molecular Genetic Advances in Fragile X Syndrome
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Late-Onset Friedreich's Ataxia, Molecular Genetics, Clinical Neurophysiology, and Magnetic Resonance Imaging
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The DNA Laboratory and Neurolgoical Practice
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Hyperkalemic Periodic Paralysis:Rapid Molecular Diag & Rela of Genotype to Phenotype in 12 Families
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Molecular Genetics in Neurology
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DNA Diagnosis of Neurofibromatosis 2:Altered Coding Sequence of the Merlin Tumor Suppressor in an Extended Pedigree
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Familial Neurofibromatosis Type 1:Clinical Experience with DNA Testing
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Screening for von Hippel-Lindau Disease by DNA Polymorphism Analysis
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Recent Progress Toward Understanding the Molecular Biology of Von Recklinghausen Neurofibromatosis
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Prenatal Diagnosis of Wilson's Disease by Analysis of DNA Polymorphism
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The First Decade of Molecular Genetics in Neurology:Changing Clinical Thought and Practice
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Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy
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Dystonia Gene in Ashkenazi Jewish Population is Located on Chromosome 9q32-34
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The Triumph of Linkage Analysis, Editorial
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Prion Dementia Without Characteristic Pathology
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Molecular Genetics of Duchenne and Becker Muscular Dystrophy
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Criteria for Establishing the Validity of Genetic Recombination in Myotonic Dystrophy
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Molecular Biology of Duchenne and Becker's Muscular Dystrophy:Clinical Applications
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The Molecular Genetic Revolution, Its Impact on Clinical Neurology
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Diagnosis of McArdle's Disease by Molecular Genetic Analysis of Blood
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Molecular Genetic Heterogeneity of Myophosphorylase Deficiency (McArdle's Disease)
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