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Muscular Dystrophies
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Clinical Reasoning: Encephalopathy in a 10-year-old boy
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A 23-Year-Old Man With Seizures and Visual Deficit
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Practice Parameter: Evaluation of the Child with Global Developmental Delay
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Diagnostic Test for the Prader-Willi Syndrome by SNRPN Expression in Blood
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Mitochondrial DNA and Disease
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Molecular Genetics of Duchenne and Becker Muscular Dystrophy
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