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A Global Haplotype Analysis of the Myotonic Dystrophy Locus: Implications for the Evolution of Modern Humans and for the Origin of Myotonic Dystrophy Mutations

✍ Scribed by S.A. Tishkoff; A. Goldman; F. Calafell; W.C. Speed; A.S. Deinard; B. Bonne-Tamir; J.R. Kidd; A.J. Pakstis; T. Jenkins; K.K. Kidd


Book ID
117852411
Publisher
American Society of Human Genetics
Year
1998
Tongue
English
Weight
548 KB
Volume
62
Category
Article
ISSN
0002-9297

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To verify the reliability of secretor status for prenatal diagnosis of myotonic dystrophy (DM), 179 amniotic fluid samples were compared with saliva or urine samples of the infants by hemagglutination inhibition. While no discrepancies were observed, problems could arise with intermediate results. A