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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
Italian Journal of Pediatrics ( IF 3.6 ) Pub Date : 2023-03-20 , DOI: 10.1186/s13052-023-01433-8
Jinying Wu 1, 2 , Meifang Lei 3 , Xuetao Wang 1, 2 , Nan Liu 1, 2 , Xiaowei Xu 1, 2 , Chunyu Gu 1, 2 , Yuping Yu 4 , Wei Liu 5
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Correction: Ital J Pediatr 48, 204 (2022)

https://doi.org/10.1186/s13052-022-01398-0

The original article [1] mistakenly mis-numbered a section of citations in the main body; this has since been rectified.

  1. Jinying W, et al. Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report. Ital J Pediatr. 2022;48:204. https://doi.org/10.1186/s13052-022-01398-0.

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Authors and Affiliations

  1. Tianjin Pediatric Research Institute, Tianjin Children’s Hospital (Children’s Hospital of Tianjin University), Tianjin, 300134, China

    Jinying Wu, Xuetao Wang, Nan Liu, Xiaowei Xu & Chunyu Gu

  2. Tianjin Key Laboratory of Birth Defects for Prevention and Treatment, Tianjin, 300134, China

    Jinying Wu, Xuetao Wang, Nan Liu, Xiaowei Xu & Chunyu Gu

  3. Department of Neurology, Tianjin Children’s Hospital (Children’s Hospital of Tianjin University), Tianjin, 300134, China

    Meifang Lei

  4. Graduate College of Tianjin Medical University, Tianjin, 300070, China

    Yuping Yu

  5. Tianjin Children’s Hospital (Children’s Hospital of Tianjin University), Tianjin, 300134, China

    Wei Liu

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  1. Jinying WuView author publications

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  2. Meifang LeiView author publications

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  3. Xuetao WangView author publications

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  6. Chunyu GuView author publications

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  7. Yuping YuView author publications

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  8. Wei LiuView author publications

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Corresponding author

Correspondence to Wei Liu.

Open Access This 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/. The Creative Commons Public Domain Dedication waiver (http://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.

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Wu, J., Lei, M., Wang, X. et al. Correction: Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report. Ital J Pediatr 49, 32 (2023). https://doi.org/10.1186/s13052-023-01433-8

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中文翻译:

更正:Prader-Willi 综合征患者因父系 15q11-q13 区域镶嵌缺失导致的非典型表型:一例报告

更正:Ital J Pediatr 48, 204 (2022)

https://doi.org/10.1186/s13052-022-01398-0

原文章[1]在正文中错误地编号了一段引文;这已经得到纠正。

  1. 金英 W 等人。父系 15q11-q13 区域镶嵌缺失导致非典型表型的 Prader-Willi 综合征患者:一例报告。意大利 J 儿科杂志。2022;48:204。https://doi.org/10.1186/s13052-022-01398-0。

    文章 CAS 谷歌学术

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作者和隶属关系

  1. 天津市儿童医院(天津大学附属儿童医院)天津市儿科研究所,天津,300134

    Jinying Wu, Xuetao Wang, Nan Liu, Xiaowei Xu & Chunyu Gu

  2. 天津市出生缺陷防治重点实验室, 天津, 300134

    Jinying Wu, Xuetao Wang, Nan Liu, Xiaowei Xu & Chunyu Gu

  3. 天津市儿童医院(天津大学附属儿童医院)神经内科,天津,300134

    雷美芳

  4. 天津医科大学研究生院,天津,300070

    余玉萍

  5. 天津市儿童医院(天津大学附属儿童医院),天津 300134

    刘伟

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Wu, J., Lei, M., Wang, X.等。更正:Prader-Willi 综合征患者因父系 15q11-q13 区域镶嵌缺失引起的非典型表型:病例报告。Ital J Pediatr 49 , 32 (2023)。https://doi.org/10.1186/s13052-023-01433-8

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更新日期:2023-03-21
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