A gene for usher syndrome type I (USH1A) maps to chromosome 14q
- 31 December 1992
- Vol. 14 (4), 979-987
- https://doi.org/10.1016/s0888-7543(05)80120-x
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Clinical and genetic heterogeneity in retinitis pigmentosaHuman Genetics, 1990
- Mapping recessive ophthalmic diseases: Linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1qGenomics, 1990
- Localization of Usher syndrome type II to chromosome 1qGenomics, 1990
- Frequent recombination is observed in the distal end of the long arm of chromosome 14Genomics, 1989
- Abnormal Sperm and Photoreceptor Axonemes in Usher's SyndromeArchives of Ophthalmology (1950), 1986
- Removal of repeated sequences from hybridisation probesNucleic Acids Research, 1985
- Usher's SyndromeArchives of Ophthalmology (1950), 1983
- Usher syndrome: Definition and estimate of prevalence from two high-risk populationsJournal of Chronic Diseases, 1983
- Increased incidence of abnormal nasal cilia in patients with retinitis pigmentosaNature, 1979
- Kartagener's Syndrome and Deaf-Mutism: An Unusual AssociationChest, 1973