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Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia (Osler-Wever-Rendu Disease)
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Spinal Muscular Atrophy
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Recurrent Cerebral Ischemia During Pregnancies
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Ehlers-Danlos Syndromes
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Molybdenum Cofactor Deficiency
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Genetic Aspects of Alzheimer Disease
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Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
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The Tuberous Sclerosis Complex
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Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Analysis of Prenatal and Gestational Care Given to Women with Epilepsy
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Practice Parameter,Management Issues for Women with Epilepsy (Summary Statement)
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The Clinical Introduction of Genetic Testing for Alzheimer Disease, An Ethical Perspective
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Apolipoprotein E Genotyping in Alzheimer's Disease
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Practice Parameter:Genetic Testing Alert
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Statement of Use of Apolipoprotein E Testing for Alzheimer Disease
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Clinical Genetics in Neurological Disease
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Myotonic Dystrophy
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Causal Heterogeneity in Isolated Lissencephaly
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The Psychological Consequences of Predictive Testing for Huntington's Disease
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Anderson-Fabray Disease, A Commonly Missed Diagnosis
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