Correction: Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report

Bibliographic Details
Main Authors: Jinying Wu, Meifang Lei, Xuetao Wang, Nan Liu, Xiaowei Xu, Chunyu Gu, Yuping Yu, Wei Liu
Format: Article
Language:English
Published: BMC 2023-03-01
Series:Italian Journal of Pediatrics
Online Access:https://doi.org/10.1186/s13052-023-01433-8
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author Jinying Wu
Meifang Lei
Xuetao Wang
Nan Liu
Xiaowei Xu
Chunyu Gu
Yuping Yu
Wei Liu
author_facet Jinying Wu
Meifang Lei
Xuetao Wang
Nan Liu
Xiaowei Xu
Chunyu Gu
Yuping Yu
Wei Liu
author_sort Jinying Wu
collection DOAJ
first_indexed 2024-04-09T22:44:28Z
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institution Directory Open Access Journal
issn 1824-7288
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publishDate 2023-03-01
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series Italian Journal of Pediatrics
spelling doaj.art-12b5899454364fa3ac27b797f910235c2023-03-22T11:54:45ZengBMCItalian Journal of Pediatrics1824-72882023-03-014911110.1186/s13052-023-01433-8Correction: Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case reportJinying Wu0Meifang Lei1Xuetao Wang2Nan Liu3Xiaowei Xu4Chunyu Gu5Yuping Yu6Wei Liu7Tianjin Pediatric Research Institute, Tianjin Children’s Hospital (Children’s Hospital of Tianjin University)Department of Neurology, Tianjin Children’s Hospital (Children’s Hospital of Tianjin University)Tianjin Pediatric Research Institute, Tianjin Children’s Hospital (Children’s Hospital of Tianjin University)Tianjin Pediatric Research Institute, Tianjin Children’s Hospital (Children’s Hospital of Tianjin University)Tianjin Pediatric Research Institute, Tianjin Children’s Hospital (Children’s Hospital of Tianjin University)Tianjin Pediatric Research Institute, Tianjin Children’s Hospital (Children’s Hospital of Tianjin University)Graduate College of Tianjin Medical UniversityTianjin Children’s Hospital (Children’s Hospital of Tianjin University)https://doi.org/10.1186/s13052-023-01433-8
spellingShingle Jinying Wu
Meifang Lei
Xuetao Wang
Nan Liu
Xiaowei Xu
Chunyu Gu
Yuping Yu
Wei Liu
Correction: Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report
Italian Journal of Pediatrics
title Correction: Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report
title_full Correction: Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report
title_fullStr Correction: Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report
title_full_unstemmed Correction: Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report
title_short Correction: Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report
title_sort correction prader willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11 q13 region a case report
url https://doi.org/10.1186/s13052-023-01433-8
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