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A Neonate with Micrognathia and Hypotonia
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Newborn Screening for Fragile X Syndrome
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Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
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Few Psychological Consequences of Presymptomatic Testing for Huntington Disease
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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The Neurogenetic Genie:Testing for Huntington's Disease Mutation
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A Worldwide Study of the Huntington's Disease Mutation, The Sensitivity & Specificity of Measuring CAG Repeats
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Myotonic Dystrophy
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Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test
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