Carrier detection in X-linked ocular albinism of the Nettleship-Falls type by DNA analysis-Reference-Cited by-同舟云学术

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Carrier detection in X-linked ocular albinism of the Nettleship-Falls type by DNA analysis

Published:2008-06-28 Issue:3 Volume:41 Page:135-138
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Bergan A. A. B.,Schuurman L J. M.,Born L. I.,Samanns G.,Dorp D. B.,Pinckers A. J. L. G.,Bakker E.,Ommen G. J. B.,Gal A.,Bleeker-Wagemakers E. M.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1992.tb03649.x/fullpdf

Reference19 articles.

1. Genetic mapping of 12 marker loci in the Xp22.3-p21.1 region;Alitalo;Hum Genet,1991

2. A decisive electrophysiological test for human albinism;Apkarian;Electroenceph Clin Neurophys,1983

3. Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLP's;Bakker;Lancet,1985

4. Molecular heterogeneity of steroid sulfatase deficiency: a multicenter study of 57 unrelated patients, at DNA and protein levels;Ballabio;Genomics,1989a

5. Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome;Ballabio;Proc Natl Acad Sci,1989b

Cited by 3 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. New mutations identified in the ocular albinism type 1 gene;Gene;2007-11

2. Lexikalischer Teil;Lexikon der Syndrome und Fehlbildungen;2003

3. Lexikon der Syndrome und Fehlbildungen;Lexikon der Syndrome und Fehlbildungen;1999

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