Novel rapid molecular diagnosis methods for comprehensive genetic analysis of 21-hydroxylase deficiency
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
-
Englisch
- Bibliographic citation
-
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
- Creator
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Xia, Yanjie
Yu, Feng
Bai, Ying
Jiang, Lili
Shi, Panlai
Jiang, Zhengwen
Kong, Xiangdong
- Contributor
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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
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:24 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
- Xia, Yanjie
- Yu, Feng
- Bai, Ying
- Jiang, Lili
- Shi, Panlai
- Jiang, Zhengwen
- Kong, Xiangdong
- SpringerLink (Online service)
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Diagnosis of female 17α-hydroxylase deficiency after gonadectomy: a case report
Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
An unusual presentation of tyrosine hydroxylase deficiency
Diagnosis of autism in a rare case of tyrosine hydroxylase deficiency: a case report
POR polymorphisms are associated with 21 hydroxylase deficiency
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