Correction: Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report
Main Authors: | , , , , , , , |
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Format: | Article |
Language: | English |
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BMC
2023-03-01
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Series: | Italian Journal of Pediatrics |
Online Access: | https://doi.org/10.1186/s13052-023-01433-8 |
_version_ | 1797863996575973376 |
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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 |
format | Article |
id | doaj.art-12b5899454364fa3ac27b797f910235c |
institution | Directory Open Access Journal |
issn | 1824-7288 |
language | English |
last_indexed | 2024-04-09T22:44:28Z |
publishDate | 2023-03-01 |
publisher | BMC |
record_format | Article |
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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