Deletion of chromosome 11 (p11p13) in a patient with Beckwith-Wiedemann syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1986.tb00588.x/fullpdf
Reference10 articles.
1. Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainment;Fraccaro;Hum. Genet.,1983
2. Trisomy 11p15 and Beckwith-Wiedemann syndrome;Journel;Ann. Genet.,1985
3. The cytogenetic controversy in the Prader-Labhart-Willi syndrome;Kouseff;Am. J. Med. Genet.,1982
4. Autosomal-dominant sex-dependent transmission of the Wiedemann-Beckwith syndrome;Lubinsky;Lancet,1974
5. Prader-Willi syndrome and chromosome 15;Mattei;Hum. Genet.,1983
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3. Identification of 11p14.1-p15.3 deletion probably associated with short stature, relative macrocephaly, and delayed closure of the fontanelles;American Journal of Medical Genetics Part A;2016-09-23
4. Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndrome.;Journal of Medical Genetics;1997-10-01
5. A complex chromosome translocation resulting in deletion 11 p and associated with uveal colobomata;Ophthalmic Genetics;1995-01
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