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

Corrigendum: Chromosomal abnormalities and pregnancy outcomes for fetuses with gastrointestinal tract obstructions

  • 1. Department 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

  • 2. Fujian Provincial Key Laboratory for Prenatal Diagnosis and Birth Defect, Fuzhou, China

  • 3. Department of Laboratory Medicine, Fujian Medical University, Fuzhou, China

  • 4. Department of Pediatrics, Guangxi Medical University, Nanning, China

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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.

Summary

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

06 October 2022

Published

26 October 2022

Volume

10 - 2022

Updates

Copyright

*Correspondence: Na Lin Hailong Huang Liangpu Xu

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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All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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