Carrier status diagnosis in Duchenne muscular dystrophy with "conformational" DNA polymorphism
- 11 January 1992
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 339 (8785) , 134
- https://doi.org/10.1016/0140-6736(92)91053-b
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- PCR-SSCP: a simple and sensitive method for detection of mutations in the genomic DNA.Genome Research, 1991
- Molecular genetics of Duchenne and Becker muscular dystrophyThe Journal of Pediatrics, 1990
- Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reactionGenomics, 1989
- Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplificationNucleic Acids Research, 1988