Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1824-7288
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
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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
- Urheber
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Wu, Jinying
Lei, Meifang
Wang, Xuetao
Liu, Nan
Xu, Xiaowei
Gu, Chunyu
Yu, Yuping
Liu, Wei
- Beteiligte Personen und Organisationen
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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
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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14.08.2025, 10:45 MESZ
Datenpartner
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Beteiligte
- Wu, Jinying
- Lei, Meifang
- Wang, Xuetao
- Liu, Nan
- Xu, Xiaowei
- Gu, Chunyu
- Yu, Yuping
- Liu, Wei
- SpringerLink (Online service)
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