Corrigendum: Chromosomal abnormalities and pregnancy outcomes for fetuses with gastrointestinal tract obstructions
Xiaoqing Wu1,2,3 
Linjuan Su1,2 Qingmei Shen1,2 Qun Guo1,2 Ying Li1,2 Shiyi Xu4 Na Lin1,2* 
Hailong Huang1,2* Liangpu Xu1,2*
- 1Department of Medical Genetic Diagnosis and Therapy Center, Fujian Maternity and Child Health Hospital, College of Clinical Medicine for Obstetrics and Gynecology and Pediatrics, Fujian Medical University, Fuzhou, China
- 2Fujian Provincial Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou, China
- 3Department of Laboratory Medicine, Fujian Medical University, Fuzhou, China
- 4Department of Pediatrics, Guangxi Medical University, Nanning, China
A corrigendum on
By Wu X, Su L, Shen Q, Guo Q, Li Y, Xu S, Lin N, Huang H and Xu L. (2022) Front. Pediatr. 10: 918130. doi: 10.3389/fped.2022.918130
In the published article, there was a mistake in affiliation of author Na Lin. His affiliation has been corrected from “5 Medical Genetic Diagnosis and Therapy Center, Fujian Provincial Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fuzhou, China” to “1 Medical Genetic Diagnosis and Therapy Center Fujian Maternity and Child Health Hospital College of Clinical Medicine for Obstetrics / Gynecology and Pediatrics, Fujian Medical University, Fuzhou, Fujian, China.” and “2 Fujian Provincial Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou, Fujian, China.”
The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.
Keywords: gastrointestinal tract obstructions, traditional karyotyping, chromosomal abnormalities, chromosomal microarray analysis, down syndrome, copy number variants
Citation: Wu X, Su L, Shen Q, Guo Q, Li Y, Xu S, Lin N, Huang H and Xu L (2022) Corrigendum: Chromosomal abnormalities and pregnancy outcomes for fetuses with gastrointestinal tract obstructions. Front. Pediatr. 10:976997. doi: 10.3389/fped.2022.976997
Received: 24 June 2022; Accepted: 6 October 2022;
Published: 26 October 2022.
Approved By:
Frontiers in Pediatrics, Frontiers Media SA, Switzerland
© 2022 Wu, Su, Shen, Guo, Li, Xu, Lin, Huang and Xu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Na Lin 846519465@qq.com Hailong Huang huanghailong@fjmu.edu.cn Liangpu Xu xiliangpu@fjmu.edu.cn
Specialty Section: This article was submitted to Genetics of Common and Rare Diseases, a section of the journal Frontiers in Pediatrics