Chromosome microarray analysis in the investigation of children with congenital heart disease-Reference-Cited by-同舟云学术

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Chromosome microarray analysis in the investigation of children with congenital heart disease

Published:2017-05-04 Issue:1 Volume:17 Page:
ISSN:1471-2431
Container-title:BMC Pediatrics
language:en
Short-container-title:BMC Pediatr

Author:

Wu Xiao-li,Li Ru,Fu Fang,Pan Min,Han Jin,Yang Xin,Zhang Yong-ling,Li Fa-tao,Liao Can

Funder

Science and technology project of Guangdong Province

The key project of Guangzhou Science and Information Technology Bureau

The key project of Guangzhou Health Bureau

Medical research foundation of Guangdong Province

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1186/s12887-017-0863-3.pdf

Reference49 articles.

1. van der Linde D, Konings EE, Slager MA, Witsenburg M, Helbing WA, Takkenberg JJ, et al. Birth prevalence of congenital heart disease worldwide: a systematic review and meta-analysis. J Am Coll Cardiol. 2011;58(21):2241–7.

2. Hartman RJ, Rasmussen SA, Botto LD, Riehle-Colarusso T, Martin CL, Cragan JD, et al. The contribution of chromosomal abnormalities to congenital heart defects: a population-based study. Pediatr Cardiol. 2011;32(8):1147–57.

3. Lindsay EA, Vitelli F, Su H, Morishima M, Huynh T, Pramparo T, et al. Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice. Nature. 2001;410(6824):97–101.

4. Yagi H, Furutani Y, Hamada H, Sasaki T, Asakawa S, Minoshima S, et al. Role of TBX1 in human del22q11.2 syndrome. Lancet. 2003;362(9393):1366–73.

5. Pober BR. Williams-Beuren syndrome. N Engl J Med. 2010;362(3):239–52.

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