Autosomal dominant retinitis pigmentosa: Exclusion of a gene from extensive regions of chromosomes 6, 13, 20, and 21
- 1 October 1989
- Vol. 5 (3), 612-618
- https://doi.org/10.1016/0888-7543(89)90030-x
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- A computer program to make linkage analysis with liped and linkage easier to perform and less prone to input errorsAnnals of Human Genetics, 1988
- Linkage analysis of X linked retinitis pigmentosa in the Irish population.Journal of Medical Genetics, 1988
- Analysis of linkage relationships of X-linked retinitis pigmentosa with the following Xp loci: L1.28, OTC, 754, XJ-1.1, pERT87, and C7Human Genetics, 1988
- A genetic linkage map of the human genomeCell, 1987
- Problems in detecting etiological heterogeneity in genetic disease illustrated with retinitis pigmentosaAmerican Journal of Medical Genetics, 1986
- Autosomal Dominantly Inherited Retinitis PigmentosaArchives of Ophthalmology (1950), 1985
- A study of retinitis pigmentosa in the City of Birmingham. I Prevalence.Journal of Medical Genetics, 1984
- Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28Nature, 1984
- Prevalence of Retinitis Pigmentosa in MaineAmerican Journal of Ophthalmology, 1984
- A technique for radiolabeling DNA restriction endonuclease fragments to high specific activityAnalytical Biochemistry, 1983