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Correction: Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report
| Autores principales: | , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10029287/ https://www.ncbi.nlm.nih.gov/pubmed/36941634 http://dx.doi.org/10.1186/s13052-023-01433-8 |
| _version_ | 1784910109271392256 |
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| author | Wu, Jinying Lei, Meifang Wang, Xuetao Liu, Nan Xu, Xiaowei Gu, Chunyu Yu, Yuping Liu, Wei |
| author_facet | Wu, Jinying Lei, Meifang Wang, Xuetao Liu, Nan Xu, Xiaowei Gu, Chunyu Yu, Yuping Liu, Wei |
| author_sort | Wu, Jinying |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-10029287 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2023 |
| publisher | BioMed Central |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-100292872023-03-22 Correction: Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report Wu, Jinying Lei, Meifang Wang, Xuetao Liu, Nan Xu, Xiaowei Gu, Chunyu Yu, Yuping Liu, Wei Ital J Pediatr Correction BioMed Central 2023-03-20 /pmc/articles/PMC10029287/ /pubmed/36941634 http://dx.doi.org/10.1186/s13052-023-01433-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
| spellingShingle | Correction Wu, Jinying Lei, Meifang Wang, Xuetao Liu, Nan Xu, Xiaowei Gu, Chunyu Yu, Yuping Liu, Wei Correction: Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report |
| 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 |
| topic | Correction |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10029287/ https://www.ncbi.nlm.nih.gov/pubmed/36941634 http://dx.doi.org/10.1186/s13052-023-01433-8 |
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