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A 29-Year-Old Man with Fevers and Rapidly Progressive Cranial Neuropathies
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A Rare Presentation of Whipple Disease
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Molecular Genetic Heterogeneity of Myophosphorylase Deficiency (McArdle's Disease)
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Charcot-Marie-Tooth Disease Type 1A:Association with a Spontaneous Point Mutation in the PMP22 Gene
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Molecular Genetics in Neurology
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Genetic Diagnosis of Gaucher's Disease
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Population Screening for Fragile X
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Mutation of the Prion Protein in Libyan Jews with Creutzfeldt-Jakob Disease
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Molecular Genetics of Duchenne and Becker Muscular Dystrophy
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