THE USE OF FIELD-INVERSION GEL-ELECTROPHORESIS FOR DELETION DETECTION IN DUCHENNE MUSCULAR-DYSTROPHY
- 1 May 1988
- journal article
- research article
- Vol. 42 (5), 777-780
Abstract
Deletion is a common cause of Duchenne muscular dystrophy (DMD). Field-inversion gel electrophoresis, in conjunction with Southern blot hybridization, was used to detect large SfiI DNA fragments in the DMD locus. Two unrelated boys with DMD were found to have abnormal sized DNA fragments resulting from deletions. Some of the female relatives of these patients were also shown by this method to have deletions in the DMD locus.This publication has 13 references indexed in Scilit:
- A partial deletion of the muscular dystrophy gene transmitted twice by an unaffected maleNature, 1987
- Mapping the disease phenotypeNature, 1987
- Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophyHuman Genetics, 1987
- Molecular analysis of the Duchenne muscular dystrophy region using pulsed field gel electrophoresisCell, 1987
- A physical map of 4 million bp around the Duchenne muscular dystrophy gene on the human X-chromosomeCell, 1986
- Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophyNature, 1986
- Electrophoretic Separations of Large DNA Molecules by Periodic Inversion of the Electric FieldScience, 1986
- Separation of chromosomal DNA molecules from yeast by orthogonal-field-alternation gel electrophoresisNucleic Acids Research, 1984
- Separation of yeast chromosome-sized DNAs by pulsed field gradient gel electrophoresisCell, 1984
- Detection of specific sequences among DNA fragments separated by gel electrophoresisJournal of Molecular Biology, 1975