Autosomal dominant retinitis pigmentosa: Linkage to rhodopsin and evidence for genetic heterogeneity
- 1 September 1990
- Vol. 8 (1), 35-40
- https://doi.org/10.1016/0888-7543(90)90223-h
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- no evidence for linkage between late onset autosomal dominant retinitis pigmentosa and chromosome 3 locus D3S47 (C17): Evidence for genetic heterogeneityGenomics, 1990
- A point mutation of the rhodopsin gene in one form of retinitis pigmentosaNature, 1990
- Autosomal dominant retinitis pigmentosa: Exclusion of a gene from extensive regions of chromosomes 6, 13, 20, and 21Genomics, 1989
- A computer program to make linkage analysis with liped and linkage easier to perform and less prone to input errorsAnnals of Human Genetics, 1988
- A genetic linkage map of the human genomeCell, 1987
- Structural and transcriptional properties associated with a member of a new family of conserved short dispersed repeated elements in human DNAGene, 1984
- A study of retinitis pigmentosa in the City of Birmingham. I Prevalence.Journal of Medical Genetics, 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
- Possible Assignment of a Dominant Retinitis pigmentosa Gene to ChromosomeOphthalmic Research, 1982