Full text
PDF
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Davie A. M., Emery A. E. Estimation of proportion of new mutants among cases of Duchenne muscular dystrophy. J Med Genet. 1978 Oct;15(5):339–345. doi: 10.1136/jmg.15.5.339. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Francke U., Felsenstein J., Gartler S. M., Migeon B. R., Dancis J., Seegmiller J. E., Bakay F., Nyhan W. L. The occurrence of new mutants in the X-linked recessive Lesch-Nyhan disease. Am J Hum Genet. 1976 Mar;28(2):123–137. [PMC free article] [PubMed] [Google Scholar]
- Gartler S. M., Francke U. Half chromatid mutations: transmission in humans? Am J Hum Genet. 1975 Mar;27(2):218–223. [PMC free article] [PubMed] [Google Scholar]
- LYON M. F. Gene action in the X-chromosome of the mouse (Mus musculus L.). Nature. 1961 Apr 22;190:372–373. doi: 10.1038/190372a0. [DOI] [PubMed] [Google Scholar]
- Lenz W. Letter: Half chromatid mutations may explain incontinentia pigmenti in males. Am J Hum Genet. 1975 Sep;27(5):690–691. [PMC free article] [PubMed] [Google Scholar]
- Roses A. D., Roses M. J., Miller S. E., Hull K. L., Jr, Appel S. H. Carrier detection in Duchenne muscular dystrophy. N Engl J Med. 1976 Jan 22;294(4):193–198. doi: 10.1056/NEJM197601222940404. [DOI] [PubMed] [Google Scholar]
- Yasuda N., Kondô K. No sex difference in mutations rates of Duchenne muscular dystrophy. J Med Genet. 1980 Apr;17(2):106–111. doi: 10.1136/jmg.17.2.106. [DOI] [PMC free article] [PubMed] [Google Scholar]