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Spinal Muscular Atrophy A Timely Review
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Neuroblastoma -- from Genetic Profiles to Clinical Challenge
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
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New Developments in the Neurobiology of the Tuberous Sclerosis Complex
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From Enigmatic to Problematic:The New Molecular Genetics of Childhood Spinal Muscular Atrophy
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Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
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The Molecular Genetic Revolution, Its Impact on Clinical Neurology
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Prenatal Genetic Diagnosis in 3000 Amniocenteses
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