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X-Linked Pure Familial Spastic Paraparesis
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Rapid Antibody Test for Fragile X Syndrome
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Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
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Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
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Clinical Significance of Fetal Choroid Plexus Cysts
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Spinocerebellar Ataxias and Ataxins
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Familial Subarachnoid Hemorrhage:Distinctive Features and Patterns of Inheritance
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Familial Hemiplegic Migraine and Autosomal Dominant Arteriopathy with Leukoencephalopathy (CADASIL)
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Clinical Spectrum of CADASIL:A Study of 7 Families
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New Phenotype of the Cerebral Autosomal Dominant Arteriopathy Mapped to Chromosome 19:Migraine as the Prominent Clinical Feature
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Statement of Use of Apolipoprotein E Testing for Alzheimer Disease
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Hereditary Hemorrhagic Telangiectasia
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The Nondystrophic Myotonias
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Superoxide Dismutase and ALS
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Trinucleotide Repeat Expansion in Neurological Disease
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On the Inheritance of Intracranial Aneurysms
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Reduced Basal Ganglia Volume Associated with the Gene for Huntington's Disease in Asymptomatic at-Risk Persons
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Neurovascular Manifestations of Heritable Connective Tissue Disorders:A Review
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Progressive Multifocal Leukoencephalopathy Complicating Wiskott-Aldrich Syndrome
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Progress in the Genetics of Cerebrovascular Disease Inherited Subcortical Arteriopathies
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The Neurogenetic Genie:Testing for Huntington's Disease Mutation
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A Worldwide Study of the Huntington's Disease Mutation, The Sensitivity & Specificity of Measuring CAG Repeats
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Clin & Path Features of an Autosomal Dominant, Adult-Onset Leukodystrophy Simul Chronic Progressive MS
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Increased Risk of Alzheimer's Disease in Mothers of Adults with Down's Syndrome
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Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
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Chromosome 14-Encoded Alzheimer's Disease:Genetic and Clinicopathological Description
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Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
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Benign Familial Disease with Muscle Mounding and Rippling
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Turcot's Syndrome:Evidence for Linkage to the Adenomatous Polyposis Coli (APC) Locus
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Increased Risk of Parkinson's Disease in Parents and Siblings of Patients
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Myotonic Dystrophy
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Familial Atrioventricular Septal Defect:Possible Genetic Mechanisms
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Liver Transplantation as a Treatment for Familial Amyloidotic Polyneuropathy
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Cerebrotendinous Xanthomatosis:Molecular Diagnosis Enables Presymptomatic Detection of a Treatable Disease
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Congential Deficienty of Factor VII in Subarachnoid Hemorrhage
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Cerebral Involvement in McLeod Syndrome
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The British Isles Survey of Multiple Sclerosis in Twins
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Clinical Genetics in Neurological Disease
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Myotonic Dystrophy with No Trinucleotide Repeat Expansion
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Familial Autoimmune Myasthenia Gravis
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Advances in Molecular Analysis of Fragile X Syndrome
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Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test
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Tay-Sachs Disease-Carrier Screening, Prenatal Diagnosis, and the Molecular Era
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X-Chromosome Effects on Female Brain:A Magnetic Resonance Imaging Study of Turner's Syndrome
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Progr Myoclonus Epilepsy of Unverricht-Lundborg Type:Clin & Molecular Genetic Study from US 4 Affected Sibs
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