- Devriendt K, Matthijs G, Claes S, Legius E, Proesmans W, Cassiman J J, Fryns J P.: Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysis. J. Med. Genet. 34:318-322, 1997. [PMC free article: PMC1050920] [PubMed: 9138157]The patient was 3.3 years old.Blood=47,XXX,upd(15)mat.,Skin fibroblasts=47,XXX(50%)/47,XX,+15MIM#: 176270
Publication Details
Copyright
Copyright © 2011-2013, Digamber
Borgaonkar.
Publisher
National Center for Biotechnology Information (US), Bethesda (MD)
NLM Citation
Borgaonkar DS. Chromosomal Variation in Man: A Catalog of Chromosomal Variants and Anomalies: Online NLM Version [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 1975-. 47,XXX/47,XX,+15.