The gene for incontinentia pigmenti: failure of linkage studies using DNA probes to confirm cytogenetic localization
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1988.tb02607.x/fullpdf
Reference21 articles.
1. A strategy to reveal high-frequency RFLPs along the human X chromosome;Aldridge;Am. J. Hum. Genet.,1984
2. X;15 translocation in a retarded girl: X inactivation pattern and attempt to localise the hexosaminidase A and other loci;Bernstein;J. Med. Genet.,1979
3. Gene for incontinentia pigmenti maps to band Xp11 with an (X;10) (qll;q12) translocation;Cannizzarro;Clin. Genet.,1987
4. An anonymous single copy X-chromosome clone DXS94 from Xq11-q21 identifies a common RFLP;Davatelis;Nucl. Acids Res.,1987
5. Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome;Davies;Nucl. Acids Res.,1983
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