Molecular Genetic Advances in Fragile X Syndrome
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Molecular Genetics in Neurology
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Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test
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Detection of Full Fragile X Mutation
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Population Screening for Fragile X
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
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Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts & Leukoencephalopathy (CADASIL)
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Adrenoleukodystrophy
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Few Psychological Consequences of Presymptomatic Testing for Huntington Disease
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