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Molecular and Clinical Implications of Variant Repeats in Myotonic Dystrophy Type 1.
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Brief report: reverse mutation in myotonic dystrophy.
N Engl J Med. 1993 Feb 18;328(7):476-80. doi: 10.1056/NEJM199302183280705.
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Direct diagnosis of myotonic dystrophy with a disease-specific DNA marker.
N Engl J Med. 1993 Feb 18;328(7):471-5. doi: 10.1056/NEJM199302183280704.
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No imprinting involved in the expression of DM-kinase mRNAs in mouse and human tissues.
Hum Mol Genet. 1993 Aug;2(8):1221-7. doi: 10.1093/hmg/2.8.1221.
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(CTG)n triplet mutation and phenotype manifestations in myotonic dystrophy patients.
Biochem Med Metab Biol. 1993 Aug;50(1):85-92. doi: 10.1006/bmmb.1993.1049.

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