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
- ISSN
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1824-7288
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report ; volume:48 ; number:1 ; day:29 ; month:12 ; year:2022 ; pages:1-6 ; date:12.2022
The Italian journal of pediatrics ; 48, Heft 1 (29.12.2022), 1-6, 12.2022
- 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/s13052-022-01398-0
- URN
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urn:nbn:de:101:1-2023031021261838469614
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:45 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
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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