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Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
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Central Nervous System Lesions in von Hippel-Lindau Syndrome
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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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Familial Paroxysmal Dystonic Choreoathetosis,Clinical Findings in a Large Japanese Family and Genetic Linkage to 2q
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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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Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
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Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus
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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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Dystonia Gene in Ashkenazi Jewish Population is Located on Chromosome 9q32-34
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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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Prion Dementia Without Characteristic Pathology
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Retinitis Pigmentosa
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