- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1750-1172
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Kallmann syndrome with FGFR1 and KAL1 mutations detected during fetal life ; volume:10 ; number:1 ; day:9 ; month:6 ; year:2015 ; pages:1-7 ; date:12.2015
Orphanet journal of rare diseases ; 10, Heft 1 (9.6.2015), 1-7, 12.2015
- Creator
-
Sarfati, Julie
Bouvattier, Claire
Bry-Gauillard, Hélène
Cartes, Alejandra
Bouligand, Jérôme
Young, Jacques
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s13023-015-0287-9
- URN
-
urn:nbn:de:101:1-2019090506242020938342
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:31 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
- Sarfati, Julie
- Bouvattier, Claire
- Bry-Gauillard, Hélène
- Cartes, Alejandra
- Bouligand, Jérôme
- Young, Jacques
- SpringerLink (Online service)
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FGF2/FGFR1 regulates autophagy in FGFR1-amplified non-small cell lung cancer cells
Expanding the mutational spectrum of monogenic hypogonadotropic hypogonadism: novel mutations in ANOS1 and FGFR1 genes
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Effects of FGFR1 Gene Polymorphisms on the Risk of Breast Cancer and FGFR1 Protein Expression
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FGFR1 wild-type rosette-forming glioneuronal tumours
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Kallmann
Mutation spectrum of Kallmann syndrome: identification of five novel mutations across ANOS1 and FGFR1
Activating FGFR1 Mutations in Sporadic Pheochromocytomas
Mutations within FGFR1 are associated with superior outcome in a series of 83 diffuse midline gliomas with H3F3A K27M mutations
FGF2/FGFR1 regulates autophagy in FGFR1-amplified non-small cell lung cancer cells
Expanding the mutational spectrum of monogenic hypogonadotropic hypogonadism: novel mutations in ANOS1 and FGFR1 genes
TRPV4 and KRAS and FGFR1 gain-of-function mutations drive giant cell lesions of the jaw
Effects of FGFR1 Gene Polymorphisms on the Risk of Breast Cancer and FGFR1 Protein Expression
FGFR1-Expression und Genkopienanzahl beim Lungenkarzinom
Untersuchung des unterschiedlichen Therapieansprechens FGFR1-amplifizierter Lungenkrebszellen
FGFR1 wild-type rosette-forming glioneuronal tumours
FGFR1-ERK1/2-SOX2 axis promotes cell proliferation, epithelial–mesenchymal transition, and metastasis in FGFR1-amplified lung cancer
Kallmann
Mutation spectrum of Kallmann syndrome: identification of five novel mutations across ANOS1 and FGFR1
Activating FGFR1 Mutations in Sporadic Pheochromocytomas
Mutations within FGFR1 are associated with superior outcome in a series of 83 diffuse midline gliomas with H3F3A K27M mutations
FGF2/FGFR1 regulates autophagy in FGFR1-amplified non-small cell lung cancer cells
Expanding the mutational spectrum of monogenic hypogonadotropic hypogonadism: novel mutations in ANOS1 and FGFR1 genes
TRPV4 and KRAS and FGFR1 gain-of-function mutations drive giant cell lesions of the jaw
Effects of FGFR1 Gene Polymorphisms on the Risk of Breast Cancer and FGFR1 Protein Expression
FGFR1-Expression und Genkopienanzahl beim Lungenkarzinom
Untersuchung des unterschiedlichen Therapieansprechens FGFR1-amplifizierter Lungenkrebszellen
FGFR1 wild-type rosette-forming glioneuronal tumours
FGFR1-ERK1/2-SOX2 axis promotes cell proliferation, epithelial–mesenchymal transition, and metastasis in FGFR1-amplified lung cancer