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Primary Adhalin Deficiency as a Cause of Muscular Dystrophy in Patients with Normal Dystrophin
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Myoblast Transfer in the Tratment of Duchenne's Muscular Dystrophy
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Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
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Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
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The Nondystrophic Myotonias
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Intestinal Pseudo-Obstruction in Adult Spinal Muscular Atrophy
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Cyclosporine Increases Muscular Force Generation in Duchenne Muscular Dystrophy
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Direct Diagnosis of Myotonic Dystrophy with a Disease-Specific DNA Marker
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Brief Report:Reverse Mutation in Myotonic Dystrophy
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Mosaic Express of Dystrophin in Carriers of Becker's Muscular Dyst & X-Linked Synd of Myalgia & Cramps
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Dystrophinopathy in Isolated Cases of Myopathy in Females
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Detection of Duchenne and Becker MD Carriers by Quant Multiplex Polymerase Chain Reaction
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Oculomotor, Auditory, and Vestib ular Responses in Myotonic Dystrophy
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Unstable DNA Sequence in Myotonic Dystrophy
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Phenotypic Expression of the Myotonic Dystrophy Gene in Monozygotic Twins
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Werdnig-Hoffman Disease & Chronic Distal Spinal Muscular Atrophy with Apparent Autosomal Dom Inherit
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The Heart in Myotonic Dystrophy
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Hearing Loss in Facioscapulohumeral Muscular Dystrophy
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Clinical & Laboratory Findings in the Oculocerebrorenal Syndrome of Lowe, with Special Ref to Growth & Renal Function
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Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
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