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Central Nervous System Lesions in von Hippel-Lindau Syndrome
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Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
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Prenatal Diagnosis of Fragile X Syndrome by Direct Detection of the Unstable DNA Sequence
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Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
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The Molecular Genetic Revolution, Its Impact on Clinical Neurology
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