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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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Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
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Alexander Disease, Ventricular Garlands and Abnormalities of the Medulla and Spinal Cord
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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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Mapping of Hereditary Neuralgic Amyotrophy (Familial Brachial Plexus Neuropathy) to Distal Chromosome 17q
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Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
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DNA Analysis in Finnish Patients with Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)
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Late-Onset Friedreich's Ataxia, Molecular Genetics, Clinical Neurophysiology, and Magnetic Resonance Imaging
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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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Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
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Central Nervous System Lesions in von Hippel-Lindau Syndrome
JNNP 55:898-901, Neumann,H.P.H.,et al, 1992
Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
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Neurofibromatosis 2 (Bilateral Acoustic Neurofibromatosis) An Update
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Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
Lancet 336:271-273, Melki,J.,et al, 1990
Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
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The Molecular Genetic Revolution, Its Impact on Clinical Neurology
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Retinitis Pigmentosa
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