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Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
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Brain Imaging in Myotonic Dystrophy Type 1
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New Nomenclature and DNA Testing Guidelines for Myotonic Dystrophy Type 1 (DM1)
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Proton Spectroscopy in Myotonic Dystrophy, Correlations with CTG Repeats
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Investigation of Muscle Disease
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Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
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Cardiac Involvement in a Large Kindred with Myotonic Dystrophy:Quant Assess & Relation to Size of CTG Repeat Expansion
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Proximal Myotonic Myopathy Syndrome in the Absence of Trinucleotide Repeat Expansions
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Myotonic Dystrophy with No Trinucleotide Repeat Expansion
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Trinucleotide Repeat Expansion in Neurological Disease
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Myotonic Dystrophy
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Direct Diagnosis of Myotonic Dystrophy with a Disease-Specific DNA Marker
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Cerebral Abnormalities in Myotonic Dystrophy
Arch Neurol 50:917-923, Chang,L.,et al, 1993
The Polymerase Chain Reaction:Application to Nervous System Disease
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Oculomotor, Auditory, and Vestib ular Responses in Myotonic Dystrophy
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Presymptomatic and Prenatal Diagnosis in Myotonic Dystrophy by Genetic Linkage Studies
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Criteria for Establishing the Validity of Genetic Recombination in Myotonic Dystrophy
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Magnetic Resonance Imaging and Clinical Correlates of Intellectual Impairment in Myotonic Dystrophy
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Central Nervous System Magnetic Resonance Imaging Findings in Myotonic Dystrophy
Arch Neurol 45:36-37, Glantz,R.H.,et al, 1988
Peripheral Neuropathy in Myotonic Dystrophy:A Nerve Biopsy Study
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The Molecular Genetic Revolution, Its Impact on Clinical Neurology
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Genetic Linkage in Neurologic Diseases
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Cerebral Ischemia with Mitral Valve Prolapse
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Peripheral Neuropathy in Myotonic Dystrophy
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Electrodiagnosis of Neuromuscular Disease
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Early Recognition of Heterozygotes for the Gene for Dystrophia Myotonica
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