Uptake of Presymptomatic Predictive Testing for Huntington's Disease
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Predictive Testing for Huntington's Disease with Use of a Linked DNA Marker
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Genetic Linkage in Neurologic Diseases
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A Simplified Six-Item Checklist for Screening for Fragile X Syndrome in the Pediatric Population
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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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De-Novo Mutation in Hereditary Motor and Sensory Neuropathy Type I
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Dystonia Gene in Ashkenazi Jewish Population is Located on Chromosome 9q32-34
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Genetic Testing for Huntington's Disease
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Predictive Testing for Huntington's Disease with Linked DNA Markers
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Mutation in Cystatin C Gene Causes Hereditary Brain Hemorrhage
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Genetic Markers for Neurofibromatosis
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Retinitis Pigmentosa
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Prenatal Diagnosis & Detection of Carriers with DNA Probes in Duchenne's Muscular Dystrophy
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First-Trimester Prenatal Diagnosis for Huntington's Disease with DNA Probes
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Hereditary Motor & Sensory Neuropathy, X-Linked:A Half Century Follow-Up
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Location of the Gene for X-Linked Spinal Muscular Atrophy
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