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Parental and chromosomal origins of microdeletion and duplication syndromes involving 7q11.23, 15q11-q13 and 22q11

✍ Scribed by Thomas, N Simon; Durkie, Miranda; Potts, Gemma; Sandford, Richard; Van Zyl, Berendine; Youings, Sheila; Dennis, Nicholas R; Jacobs, Patricia A

Book ID: 110026619
Publisher: Nature Publishing Group
Year: 2006
Tongue: English
Weight: 92 KB
Volume: 14
Category: Article
ISSN: 1018-4813
DOI: 10.1038/sj.ejhg.5201617

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D u p l i c a t i o n s o f c h r o m o s o m e r e g i o n 15q11q13 often occur as a supernumerary chromosome 15. Less frequently they occur as interstitial duplications [dup(15)]. We describe the clinical and molecular characteristics of three patients with de novo dup(15). The patients, two males