Non-allelic mutations in X-linked retinitis pigmentosa-Reference-Cited by-同舟云学术

Non-allelic mutations in X-linked retinitis pigmentosa

Published:2008-06-28 Issue:5 Volume:35 Page:338-342
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Chen J. D.,Dickinson P.,Gray R.,Constable I.,Sheffield L.,Denton M. J.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1989.tb02954.x/fullpdf

Reference14 articles.

1. Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe LI.28;Bhattacharya;Nature,1984

2. X-linked retinitis pigmentosa;Bird;Br. J. Ophthalmol.,1975

3. Analysis of linkage relationships of X-linked retinitis pigmentosa with the following Xp loci: L 1.28, OTC, 754, XJ-1.1, pERT87, and C7;Denton;Hum. Genet.,1988

4. Linkage analysis of X-linked retinitis pigmentosa in the Irish population;Farrar;J. Med. Genet.,1988

5. Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome;Francke;Am. J. Hum. Genet.,1985

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genetic mapping of loci for X-linked retinitis pigmentosa;Clinical Genetics;2008-06-28

2. Glaucoma genetics, present and future;Clinical Genetics;1999-02

3. Molecular Genetics of Blindness;Molecular Genetic Medicine;1994

4. Molecular genetics of inherited retinal degenerations;Current Opinion in Genetics & Development;1992-01

5. Genetic and physical mapping around the properdin P gene;Genomics;1991-12