Structural and numerical changes of chromosome X in patients with esophageal atresia-Reference-Cited by-同舟云学术

Structural and numerical changes of chromosome X in patients with esophageal atresia

Published:2014-01-08 Issue:9 Volume:22 Page:1077-1084
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Brosens Erwin,de Jong Elisabeth M,Barakat Tahsin Stefan,Eussen Bert H,D'haene Barbara,De Baere Elfride,Verdin Hannah,Poddighe Pino J,Galjaard Robert-Jan,Gribnau Joost,Brooks Alice S,Tibboel Dick,de Klein Annelies

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg2013295.pdf

Reference56 articles.

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3. Iskender C, Tarim E, Cok T, Yalcinkaya C, Kalayci H, Sahin F : Fetal axillary cystic hygroma: a novel association with triple X syndrome. Birth Defects Res A 2012; 94: 955–957.

4. Otter M, Schrander-Stumpel CT, Curfs LM : Triple X syndrome: a review of the literature. Eur J Hum Genet 2010; 18: 265–271.

5. Visootsak J, Graham JM Jr : Klinefelter syndrome and other sex chromosomal aneuploidies. Orphanet J Rare Dis 2006; 1: 42.

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