Novel rapid molecular diagnosis methods for comprehensive genetic analysis of 21-hydroxylase deficiency
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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1 Online-Ressource.
- Sprache
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Englisch
- Erschienen in
-
Novel rapid molecular diagnosis methods for comprehensive genetic analysis of 21-hydroxylase deficiency ; volume:19 ; number:1 ; day:28 ; month:10 ; year:2024 ; pages:1-13 ; date:12.2024
Orphanet journal of rare diseases ; 19, Heft 1 (28.10.2024), 1-13, 12.2024
- Urheber
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Xia, Yanjie
Yu, Feng
Bai, Ying
Jiang, Lili
Shi, Panlai
Jiang, Zhengwen
Kong, Xiangdong
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
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10.1186/s13023-024-03414-4
- URN
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urn:nbn:de:101:1-2501172109516.854731212683
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:24 MESZ
Datenpartner
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Beteiligte
- Xia, Yanjie
- Yu, Feng
- Bai, Ying
- Jiang, Lili
- Shi, Panlai
- Jiang, Zhengwen
- Kong, Xiangdong
- SpringerLink (Online service)
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