Expanding the phenotypic spectrum of LHCGR signal peptide insertion variant: novel clinical and allelic findings causing Leydig cell hypoplasia type II
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
-
Englisch
- Bibliographic citation
-
Expanding the phenotypic spectrum of LHCGR signal peptide insertion variant: novel clinical and allelic findings causing Leydig cell hypoplasia type II ; day:25 ; month:3 ; year:2024 ; pages:1-8
Hormones ; (25.3.2024), 1-8
- Creator
-
Hassan, Heba Amin
Mazen, Inas
Elaidy, Aya
Kamel, Alaa K.
Eissa, Noura R.
Essawi, Mona L.
- Contributor
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SpringerLink (Online service)
- DOI
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10.1007/s42000-024-00546-x
- URN
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urn:nbn:de:101:1-2405271039077.545532321827
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:48 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Hassan, Heba Amin
- Mazen, Inas
- Elaidy, Aya
- Kamel, Alaa K.
- Eissa, Noura R.
- Essawi, Mona L.
- SpringerLink (Online service)
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