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Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
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Spinal Muscular Atrophy
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Molybdenum Cofactor Deficiency
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Epilepsy in Pregnancy
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Prader-Willi and Angelman Syndromes
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Practice Parameter,Management Issues for Women with Epilepsy (Summary Statement)
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Lissencephaly:A Human Brain Malformation Associated with Deletion of the LIS1 Gene Located at Chromosome 17p13
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Causal Heterogeneity in Isolated Lissencephaly
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A Clinical Study of Noonan Syndrome
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Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
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Neurological Findings in Patients with the Fragile-X Syndrome
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Fragile X Chromosome & X-Linked Mental Retardation
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