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CORRECTION article
Front. Pediatr. , 26 October 2022
Sec. Genetics of Common and Rare Diseases
Volume 10 - 2022 | https://doi.org/10.3389/fped.2022.976997
This article is a correction to:
Chromosomal Abnormalities and Pregnancy Outcomes for Fetuses With Gastrointestinal Tract Obstructions
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 ODQ2NTE5NDY1QHFxLmNvbQ== Hailong Huang aHVhbmdoYWlsb25nQGZqbXUuZWR1LmNu Liangpu Xu eGlsaWFuZ3B1QGZqbXUuZWR1LmNu
Specialty Section: This article was submitted to Genetics of Common and Rare Diseases, a section of the journal Frontiers in Pediatrics
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