Correction: Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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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 ; volume:49 ; number:1 ; day:20 ; month:3 ; year:2023 ; pages:1 ; date:12.2023
The Italian journal of pediatrics ; 49, Heft 1 (20.3.2023), 1, 12.2023
- Creator
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Wu, Jinying
Lei, Meifang
Wang, Xuetao
Liu, Nan
Xu, Xiaowei
Gu, Chunyu
Yu, Yuping
Liu, Wei
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s13052-023-01433-8
- URN
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urn:nbn:de:101:1-2023080821182029764283
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:47 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Wu, Jinying
- Lei, Meifang
- Wang, Xuetao
- Liu, Nan
- Xu, Xiaowei
- Gu, Chunyu
- Yu, Yuping
- Liu, Wei
- SpringerLink (Online service)
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