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Localization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysis.
Musarella MA, Burghes A, Anson-Cartwright L, Mahtani MM, Argonza R, Tsui LC, Worton R. Musarella MA, et al. Am J Hum Genet. 1988 Oct;43(4):484-94. Am J Hum Genet. 1988. PMID: 2902787 Free PMC article.
The X-linked recessive type of retinitis pigmentosa (XLRP) causes progressive night blindness, visual field constriction, and eventual blindness in affected males by the third or fourth decade of life. ...Heterogeneity in XLRP has been suggested by linkage st …
The X-linked recessive type of retinitis pigmentosa (XLRP) causes progressive night blindness, visual field constrictio …
Genetic linkage of Bietti crystallin corneoretinal dystrophy to chromosome 4q35.
Jiao X, Munier FL, Iwata F, Hayakawa M, Kanai A, Lee J, Schorderet DF, Chen MS, Kaiser-Kupfer M, Hejtmancik JF. Jiao X, et al. Am J Hum Genet. 2000 Nov;67(5):1309-13. doi: 10.1016/S0002-9297(07)62960-7. Epub 2000 Sep 21. Am J Hum Genet. 2000. PMID: 11001583 Free PMC article.
Bietti crystalline corneoretinal dystrophy (BCD) is an autosomal recessive retinal degeneration characterized by multiple glistening intraretinal dots scattered over the fundus, degeneration of the retina, and sclerosis of the choroidal vessels, ultimately resulting in progres …
Bietti crystalline corneoretinal dystrophy (BCD) is an autosomal recessive retinal degeneration characterized by multiple glistening intrare …
Mapping recessive ophthalmic diseases: linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q.
Lewis RA, Otterud B, Stauffer D, Lalouel JM, Leppert M. Lewis RA, et al. Genomics. 1990 Jun;7(2):250-6. doi: 10.1016/0888-7543(90)90547-8. Genomics. 1990. PMID: 1971808
Usher syndrome is a heterogeneous group of autosomal recessive disorders that combines variably severe congenital neurosensory hearing impairment with progressive night-blindness and visual loss similar to that in retinitis pigmentosa. ...The most likely loca …
Usher syndrome is a heterogeneous group of autosomal recessive disorders that combines variably severe congenital neurosensory hearing impai …