Direct molecular diagnosis of myotonic dystrophy
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1993.tb03819.x/fullpdf
Reference39 articles.
1. Anticipation in myotonic dystrophy. II. Complex relationships between clinical findings and structure of the GCT repeat;Ashizawa;Neurology,1992a
2. Anticipation in myotonic dystrophy. I. Statistical verification based on clinical and haplotype findings;Ashizawa;Neurology,1992b
3. Cloning of the essential myotonic dystrophy region and mapping of the putative defect;Aslanidis;Nature,1992
4. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member;Brook;Cell,1992
5. Presymptomatic diagnosis of myotonic dystrophy;Brunner;J Med Genet,1992
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