Retinitis pigmentosa: genetic mapping in X-linked and autosomal forms of the disease
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1990.tb03541.x/fullpdf
Reference56 articles.
1. Genetic and epidemiological investigations on pigmentary degeneration of the retina and allied disorders in Switzerland;Amman;J. Neurol. Sci.,1965
2. DNA linkage analysis of X chromosome-linked chronic granulomatous disease;Baehner;Proc. Natl. Acad. Sci. U.S.A.,1986
3. Localization of the McLeod locus (XK) within Xp21 by deletion analysis;Bertelson;Am. J. Hum. Genet.,1988
4. Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28;Bhattacharya;Nature,1984
5. Further evidence of exclusion of linkage between type II autosomal dominant retinitis pigmentosa (ADRP) and D3S47 on 3q;Blanton;Genomics,1990
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