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Obstetrics and Gynecology International
Volume 2010, Article ID 379534, 4 pages
http://dx.doi.org/10.1155/2010/379534
Case Report

Trisomy 9 Mosaicism Diagnosed In Utero

1Department of Maternal-Fetal and Neonatal Medicine, National Center for Child Health and Development, Tokyo 157-8535, Japan
2Department of Clinical Genetics and Molecular Medicine, National Center for Child Health and Development, Tokyo 157-8535, Japan

Received 1 February 2010; Accepted 23 June 2010

Academic Editor: Joe Leigh Simpson

Copyright © 2010 Hironori Takahashi et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Citations to this Article [8 citations]

The following is the list of published articles that have cited the current article.

  • Danielle Veenma, Niels Beurskens, Hannie Douben, Bert Eussen, Petra Noomen, Lutgarde Govaerts, Els Grijseels, Maarten Lequin, Ronald de Krijger, Dick Tibboel, Annelies de Klein, and Dian Van Opstal, “Comparable Low-Level Mosaicism in Affected and Non Affected Tissue of a Complex CDH Patient,” Plos One, vol. 5, no. 12, 2010. View at Publisher · View at Google Scholar
  • Chih-Ping Chen, Fang-Yu Hung, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Chen-Chi Lee, Yu-Ting Chen, Wen-Lin Chen, and Wayseen Wang, “Prenatal diagnosis of mosaic trisomy 9,” Taiwanese Journal of Obstetrics & Gynecology, vol. 50, no. 4, pp. 549–553, 2011. View at Publisher · View at Google Scholar
  • Juan A. Tovar, “Congenital Diaphragmatic Hernia,” Orphanet Journal Of Rare Diseases, vol. 7, 2012. View at Publisher · View at Google Scholar
  • Enrica Bianchi, Marco Artico, Paola Mancini, Stefania De Vito, Elena Pompili, Samanta Taurone, Isabella Guerrisi, Antonino Guerrisi, Vito D'Andrea, and Vito Cantisani, “Congenital asymptomatic diaphragmatic hernias in adults: a case series.,” Journal of medical case reports, vol. 7, pp. 125, 2013. View at Publisher · View at Google Scholar
  • Anne M. Slavotinek, “The Genetics of Common Disorders - Congenital Diaphragmatic Hernia,” European Journal of Medical Genetics, 2014. View at Publisher · View at Google Scholar
  • Zornitza Stark, Joanna Behrsin, Trent Burgess, Anna Ritchie, Alison Yeung, Tiong Y. Tan, Natasha J. Brown, Ravi Savarirayan, and Neil Patel, “SNP microarray abnormalities in a cohort of 28 infants with congenital diaphragmatic hernia,” American Journal of Medical Genetics Part A, 2015. View at Publisher · View at Google Scholar
  • Chih-Ping Chen, Yeou-Lih Wang, Wayseen Wang, Schu-Rern Chern, Yu-Peng Liu, Cheng-Ran Peng, Yu-Ling Kuo, Peih-Shan Wu, and Wen-Lin Chen, “Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diaphragmatic hernia,” Taiwanese Journal of Obstetrics and Gynecology, vol. 54, no. 1, pp. 66–70, 2015. View at Publisher · View at Google Scholar
  • Tahir Majeed, Ajaz Koul, Talib Khan, and Sahil Hassan, “Bowel sounds in the chest: An uncommon presentation of adult hernia,” Respiratory Medicine Case Reports, vol. 25, pp. 199–200, 2018. View at Publisher · View at Google Scholar