Interstitial 11q deletion derived from a maternal ins(4;11)(p14;q24.2q25): A patient report and review-Reference-Cited by-同舟云学术

Interstitial 11q deletion derived from a maternal ins(4;11)(p14;q24.2q25): A patient report and review

Published:2009-07 Issue:7 Volume:149A Page:1468-1475
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Van Zutven Laura J.C.M.,van Bever Yolande,Van Nieuwland Carolien C.M.,Huijbregts Gido C.M.,Van Opstal Diane,von Bergh Anne R.M.,Corel Linda J.A.,Tibboel Dick,Wouters Cokkie H.,Poddighe Pino J.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.32714/fullpdf

Reference25 articles.

1. Interstitial deletion of the long arm of chromosome 11;Carnevale;Ann Genet,1987

2. A de novo subtelomeric monosomy 11q (11q24.2-qter) and trisomy 20q (20q13.3-qter) in a girl with findings compatible with Jacobsen syndrome: Case report and review;Courtens;Clin Dysmorphol,2007

3. Interstitial deletion 11q. Case report and review of the literature;De Pater;Genet Couns,1997

4. Jacobsen syndrome and Beckwith-Wiedemann syndrome caused by a parental pericentric inversion inv(11)(p15q24);Gadzicki;Ann Hum Genet,2006

5. The 11q terminal deletion disorder: A prospective study of 110 cases;Grossfeld;Am J Med Genet Part A,2004

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