SHFLD3 phenotypes caused by 17p13.3 triplication/ duplication encompassing Fingerin (BHLHA9) invariably
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1750-1172
- 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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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
- Urheber
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Bukowska-Olech, Ewelina
Sowińska-Seidler, Anna
Wierzba, Jolanta
Jamsheer, Aleksander
- Beteiligte Personen und Organisationen
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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
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:22 MESZ
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Beteiligte
- Bukowska-Olech, Ewelina
- Sowińska-Seidler, Anna
- Wierzba, Jolanta
- Jamsheer, Aleksander
- SpringerLink (Online service)
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