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Hereditary Spastic Paraplegia:Advances in Genetic Research
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Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
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Molecular Genetic Advances in Fragile X Syndrome
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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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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Genetic Factors in Alzheimer's Disease:A Review of Recent Advances
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DNA Analysis in Finnish Patients with Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)
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The First Decade of Molecular Genetics in Neurology:Changing Clinical Thought and Practice
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Molecular Genetics of Duchenne and Becker Muscular Dystrophy
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Presymptomatic and Prenatal Diagnosis in Myotonic Dystrophy by Genetic Linkage Studies
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Genetic Linkage of Hereditary Motor & SensoryNeuro Type I (Charcot-Marie-Tooth Disease) to Chrom 1 & 17
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Diagnosis of Gerstmann-Straussler Syndrome in Familial Dementia with Prion Protein Gene Analysis
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