Prader-Willi syndrome in a child with a balanced (X;15) de novo translocation
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1984.tb04379.x/fullpdf
Reference13 articles.
1. Metacarpophalangeal pattern profile analysis in Prader-Willi syndrome;Butler;Clin. Genet.,1982
2. Differential binding of alkylating fluoroch-romes in human chromosomes;Caspersson;Exp. Cell. Res.,1970
3. Translocations in Prader-Will syndrome;Charrow;Clin. Genet.,1983
4. The cytogenetic controversy in the Prader-Labhart-Will syndrome;Kousseff;Am. J. Med. Genet.,1982
5. Deletions of chromosome 15 as a cause of the Prader-Willi syndrome;Ledbetter;N. Engl. J. Med.,1981
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1. ZDHHC15 as a candidate gene for autism spectrum disorder;American Journal of Medical Genetics Part A;2022-12-23
2. Prader-Willi syndrome phenocopy due to duplication of Xq21.1-q21.31, with array CGH of the critical region;Clinical Genetics;2008-02-13
3. Loss of ZDHHC15 expression in a woman with a balanced translocation t(X;15)(q13.3;cen) and severe mental retardation;European Journal of Human Genetics;2005-05-25
4. Prader-Willi syndrome: Current understanding of cause and diagnosis;American Journal of Medical Genetics;1990-03
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