8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH-Reference-Cited by-同舟云学术

8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH

Published:2007-10-17 Issue:1 Volume:16 Page:18-27
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Barber John C K,Maloney Viv K,Huang Shuwen,Bunyan David J,Cresswell Lara,Kinning Esther,Benson Anna,Cheetham Tim,Wyllie Jonathan,Lynch Sally Ann,Zwolinski Simon,Prescott Laura,Crow Yanick,Morgan Rob,Hobson Emma

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/5201932.pdf

Reference29 articles.

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2. Devriendt K, Matthijs G, Van Dael R et al: Delineation of the critical deletion region for congenital heart defects on chromosome 8p23.1. Am J Hum Genet 1999; 64: 1119–1126.

3. Shimokawa O, Miyake N, Yoshimura T et al: Molecular characterization of del(8)(p23.1p23.1) in a case of congenital diaphragmatic hernia. Am J Med Genet A 2005; 136: 49–51.

4. Slavotinek A, Lee SS, Davis R et al: Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1. J Med Genet 2005; 42: 730–736.

5. de Vries BB, Pfundt R, Leisink M et al: Diagnostic genome profiling in mental retardation. Am J Hum Genet 2005; 77: 606–616.

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