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Neonatal Seizures
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Spinal Muscular Atrophy
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Recurrent Cerebral Ischemia During Pregnancies
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Huntingtons Disease
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Prenatal Diagnosis Requests for Huntington's Disease when the Father is at Risk, and Does Not Want to Know His Genetic Status: Clinical, Legal, and Ethical Viewpoints
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New Strategy for Prenatal Diagnosis of X-Linked Disorders
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New Nomenclature and DNA Testing Guidelines for Myotonic Dystrophy Type 1 (DM1)
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Genetic Analysis Enables Definite and Rapid Diagnosis of Cerebrotendinous Xanthomatosis
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X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
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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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