SHFLD3 phenotypes caused by 17p13.3 triplication/ duplication encompassing Fingerin (BHLHA9) invariably
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1750-1172
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
-
online resource.
- Bibliographic citation
-
SHFLD3 phenotypes caused by 17p13.3 triplication/ duplication encompassing Fingerin (BHLHA9) invariably ; volume:17 ; number:1 ; day:26 ; month:8 ; year:2022 ; pages:1-8 ; date:12.2022
Orphanet journal of rare diseases ; 17, Heft 1 (26.8.2022), 1-8, 12.2022
- Creator
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Bukowska-Olech, Ewelina
Sowińska-Seidler, Anna
Wierzba, Jolanta
Jamsheer, Aleksander
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s13023-022-02480-w
- URN
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urn:nbn:de:101:1-2022111309335553662482
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:22 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
- Bukowska-Olech, Ewelina
- Sowińska-Seidler, Anna
- Wierzba, Jolanta
- Jamsheer, Aleksander
- SpringerLink (Online service)
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