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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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Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients
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Misdiagnosis Revealed by Genetic Linkage Analysis in a Family with Wilson Disease
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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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Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
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Molecular Genetic Advances in Fragile X Syndrome
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Late-Onset Friedreich's Ataxia, Molecular Genetics, Clinical Neurophysiology, and Magnetic Resonance Imaging
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The DNA Laboratory and Neurolgoical Practice
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Hyperkalemic Periodic Paralysis:Rapid Molecular Diag & Rela of Genotype to Phenotype in 12 Families
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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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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Prenatal Diagnosis of Fragile X Syndrome by Direct Detection of the Unstable DNA Sequence
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Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
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Retinitis Pigmentosa
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