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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Dystonia Gene in Ashkenazi Jewish Population is Located on Chromosome 9q32-34
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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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Neurofibromatosis 2 (Bilateral Acoustic Neuro-fibromatosis)
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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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The Molecular Genetic Revolution, Its Impact on Clinical Neurology
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Retinitis Pigmentosa
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Genetic Linkage in Neurologic Diseases
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Prenatal Diagnosis & Detection of Carriers with DNA Probes in Duchenne's Muscular Dystrophy
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The Combined Use of Positron Emission Tomography & DNA Polymorphisms for Preclinical Detection of Huntington's Disease
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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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Molecular Genetics, Recombinant DNA Techniques, & Genetic Neurological Disease
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Genetic Testing in Huntington's Disease
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Recombinant DNA & Neurologic Disease:The Coming of a New Age
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Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
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New Players in the Genetics of Stroke
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Linkiage of Locus for Cerebral Cavernous Hemagiomas to Chromosome 7q in 4 Families of Mexican-American Descent
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Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients
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Mapping of Hereditary Neuralgic Amyotrophy (Familial Brachial Plexus Neuropathy) to Distal Chromosome 17q
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Hereditary Spastic Paraplegia:Advances in Genetic Research
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Genetic Factors in Alzheimer's Disease:A Review of Recent Advances
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Confirmation of Linkage of Oculopharyngeal Muscular Dystrophy to Chromosome 14q11. 2-q13
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Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
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Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus
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Clinical Genetics in Neurological Disease
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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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Molecular Genetic Heterogeneity of Myophosphorylase Deficiency (McArdle's Disease)
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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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Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
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Recent Progress Toward Understanding the Molecular Biology of Von Recklinghausen Neurofibromatosis
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Prenatal Diagnosis of Wilson's Disease by Analysis of DNA Polymorphism
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Startle Disease, or Hyperrekplexia:Clonazepam and Assign of Gene (STHE) to Chromosoma 5q by Linkage Analysis
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Detecting Susceptibility to Malignant Hyperthermia
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Brief Report:Intragenic Deletion of the Kalig-1 Gene in Kallmann's Syndrome
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Central Nervous System Lesions in von Hippel-Lindau Syndrome
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Genetic Susceptibility to Multiple Sclerosis Linked to Myelin Basic Protein Gene
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
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Benign Familial Neonatal Convulsions:Evidence for Clinical and Genetic Heterogeneity
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The Triumph of Linkage Analysis, Editorial
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Neurofibromatosis 2 (Bilateral Acoustic Neurofibromatosis) An Update
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