Abstract
Intragenic RFLP analysis was used to provide carrier risk estimations on 100 possible female carriers from 22 Duchenne muscular dystrophy families. This enabled 78% of possible carriers to be assigned high or low risks (greater than 90% or less than 10%) as opposed to 26% assigned low risk on pedigree data alone. When a single polymorphism is not informative the use of haplotype analysis for carrier estimations is illustrated for one family.
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- Chen J. D., Denton M. J., Morgan G., Pearn J. H., Mackinlay A. G. The use of field-inversion gel electrophoresis for deletion detection in Duchenne muscular dystrophy. Am J Hum Genet. 1988 May;42(5):777–780. [PMC free article] [PubMed] [Google Scholar]
- Donald J. A., Morgan G., Chen J. D., Serravalle S., Colley P., Denton M. J. Recombination between Duchenne muscular dystrophy and DNA marker DXS164 (pERT87) Lancet. 1987 Jan 3;1(8523):39–40. doi: 10.1016/s0140-6736(87)90725-2. [DOI] [PubMed] [Google Scholar]
- Feinberg A. P., Vogelstein B. "A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum. Anal Biochem. 1984 Feb;137(1):266–267. doi: 10.1016/0003-2697(84)90381-6. [DOI] [PubMed] [Google Scholar]
- Jeanpierre M. A rapid method for the purification of DNA from blood. Nucleic Acids Res. 1987 Nov 25;15(22):9611–9611. doi: 10.1093/nar/15.22.9611. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lindlöf M., Sistonen P., de la Chapelle A. Linked polymorphic DNA markers in the prediction of X-linked muscular dystrophy. Ann Hum Genet. 1987 Oct;51(Pt 4):317–328. doi: 10.1111/j.1469-1809.1987.tb01066.x. [DOI] [PubMed] [Google Scholar]
- Old J. M., Davies K. E. Prenatal diagnosis of Duchenne muscular dystrophy by DNA analysis. J Med Genet. 1986 Dec;23(6):556–559. doi: 10.1136/jmg.23.6.556. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Read A. P., Mountford R. C., Forrest S. M., Kenwrick S. J., Davies K. E., Harris R. Patterns of exon deletions in Duchenne and Becker muscular dystrophy. Hum Genet. 1988 Oct;80(2):152–156. doi: 10.1007/BF00702859. [DOI] [PubMed] [Google Scholar]
- Southern E. M. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol. 1975 Nov 5;98(3):503–517. doi: 10.1016/s0022-2836(75)80083-0. [DOI] [PubMed] [Google Scholar]
- Worton R. G., Burghes A. H. Molecular genetics of Duchenne and Becker muscular dystrophy. Int Rev Neurobiol. 1988;29:1–76. doi: 10.1016/s0074-7742(08)60083-5. [DOI] [PubMed] [Google Scholar]

