Identification of a 220-kb insertion into the Duchenne gene in a family with an atypical course of muscular dystrophy
- 1 May 1989
- Vol. 4 (4) , 592-596
- https://doi.org/10.1016/0888-7543(89)90283-8
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- Partial gene duplication in Duchenne and Becker muscular dystrophies.Journal of Medical Genetics, 1988
- A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy geneGenomics, 1988
- Direct detection of more than 50% of the Duchenne muscular dystrophy mutations by field inversion gelsNature, 1987
- Preferential deletion of exons in Duchenne and Becker muscular dystrophiesNature, 1987
- A large inverted duplication allows homologous recombination between chromosomes heterozygous for the proximal t complex inversionCell, 1987
- Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy families.Journal of Medical Genetics, 1986
- Long-range restriction map around the Duchenne muscular dystrophy geneNature, 1986
- PRENATAL DIAGNOSIS AND CARRIER DETECTION OF DUCHENNE MUSCULAR DYSTROPHY WITH CLOSELY LINKED RFLPsThe Lancet, 1985
- Report of the committee on the genetic constitution of the X and Y chromosomesCytogenetic and Genome Research, 1985
- A technique for radiolabeling DNA restriction endonuclease fragments to high specific activityAnalytical Biochemistry, 1984