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
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.
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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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
Tianjin Key Laboratory of Birth Defects for Prevention and Treatment, Tianjin, 300134, China
Jinying Wu, Xuetao Wang, Nan Liu, Xiaowei Xu & Chunyu Gu
Department of Neurology, Tianjin Children’s Hospital (Children’s Hospital of Tianjin University), Tianjin, 300134, China
Meifang Lei
Graduate College of Tianjin Medical University, Tianjin, 300070, China
Yuping Yu
Tianjin Children’s Hospital (Children’s Hospital of Tianjin University), Tianjin, 300134, China
Wei Liu
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Correspondence to Wei Liu.
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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。
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。
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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
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
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
天津医科大学研究生院,天津,300070
余玉萍
天津市儿童医院(天津大学附属儿童医院),天津 300134
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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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