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PMID: 2878392 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Carrier diagnosis of Duchenne muscular dystrophy using restriction fragment length polymorphisms.

Neurology ·Vol. 36 ·No. 12 ·1986-12-00 ·Pages 1553-62

Hejtmancik JF, Harris SG, Tsao CC, Ward PA, Caskey CT

Abstract

Molecular probes that are tightly linked to and flank the Duchenne muscular dystrophy (DMD) locus, have been used to characterize DMD mutations and diagnose female carriers. Deletions within the Xp21 region were identified for 8 of 71 families studied. Using both DNA and CK studies, accurate (96 to 98%) carrier or noncarrier diagnoses were made for 51 of 75 females at risk in 24 families with a single affected male. DNA studies resulted in an alteration of predicted risk in 40% of the cases. Recombinant diagnostic methods are useful for carrier detection in families with one or more affected males.

MeSH Terms
Chromosome Deletion Creatine Kinase/blood DNA Restriction Enzymes/metabolism DNA, Recombinant Female Genetic Carrier Screening Genetic Linkage Genetic Markers Humans Male Muscular Dystrophies/diagnosis,enzymology,genetics Pedigree Polymorphism, Genetic Polymorphism, Restriction Fragment Length Risk
Chemicals
DNA, Recombinant Genetic Markers Creatine Kinase DNA Restriction Enzymes
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Hejtmancik J F
Harris S G
Tsao C C
Ward P A
Caskey C T
Article Info
Journal
Neurology
Abbr.
Neurology
ISSN
0028-3878
Published
1986-12-00
Pages
1553-62
Language
English
Region
United States
NLM ID
0401060
Subset
IM
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