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Molecular Genetics of Duchenne and Becker Muscular Dystrophy
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Distinction of Becker from Limb-Girdle Muscular Dystrophy by Means of Dystrophin cDNA Probes
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Molecular Biology of Duchenne and Becker's Muscular Dystrophy:Clinical Applications
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Retinitis Pigmentosa
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Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
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A Simplified Six-Item Checklist for Screening for Fragile X Syndrome in the Pediatric Population
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The First Decade of Molecular Genetics in Neurology:Changing Clinical Thought and Practice
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De-Novo Mutation in Hereditary Motor and Sensory Neuropathy Type I
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Prenatal Diagnosis of Fragile X Syndrome by Direct Detection of the Unstable DNA Sequence
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Genetic Testing for Huntington's Disease
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Genetic Abnormalities in Duchenne and Becker Dystrophies:Clinical Correlations
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Molecular and Clinical Correlations of Deletions Leading to Duchenne and Becker Muscular Dystrophies
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Prenatal Testing for Duchenne & Becker Muscular Dystrophy
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Gene Studies in Newborn Males with Duchenne Muscular Dystrophy Detected by Neonatal Screening
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Genetic Markers for Neurofibromatosis
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Hereditary Motor & Sensory Neuropathy, X-Linked:A Half Century Follow-Up
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Effective Strategy for Prenatal Prediction of Duchenne & Becker Muscular Dystrophy
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Location of the Gene for X-Linked Spinal Muscular Atrophy
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