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Unusual Variants of Alexander's Disease
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Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
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A Simplified Six-Item Checklist for Screening for Fragile X Syndrome in the Pediatric Population
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Persistence of Initial Infection in Recurrent Cryptococcus Neuformans Meningitis
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Direct Diagnosis of Myotonic Dystrophy with a Disease-Specific DNA Marker
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Screening for von Hippel-Lindau Disease by DNA Polymorphism Analysis
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The First Decade of Molecular Genetics in Neurology:Changing Clinical Thought and Practice
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Predictive Testing for Huntington's Disease with Linked DNA Markers
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Prenatal Testing for Duchenne & Becker Muscular Dystrophy
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Mutation in Cystatin C Gene Causes Hereditary Brain Hemorrhage
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