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Newborn Screening for Fragile X Syndrome
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Brugada Syndrome in Spinal and Bulbar Muscular Atrophy
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Oculopharyngeal Muscular Dystrophy in Hispanic New Mexicans
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GCG Genetic Expansions in Italian Patients with Oculopharyngeal Muscular Dystrophy
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New Nomenclature and DNA Testing Guidelines for Myotonic Dystrophy Type 1 (DM1)
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