Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patients
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1897-4287
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patients ; volume:14 ; number:1 ; day:8 ; month:6 ; year:2016 ; pages:1-7 ; date:12.2016
Hereditary cancer in clinical practice ; 14, Heft 1 (8.6.2016), 1-7, 12.2016
- Creator
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Bennedbæk, Marc
- Contributor
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Rossing, Maria
Rasmussen, Åse K.
Gerdes, Anne-Marie
Skytte, Anne-Bine
Jensen, Uffe B.
Nielsen, Finn C.
Hansen, Thomas v. O.
SpringerLink (Online service)
- DOI
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10.1186/s13053-016-0053-6
- URN
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urn:nbn:de:1111-2016060915045
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 11:04 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
- Bennedbæk, Marc
- Rossing, Maria
- Rasmussen, Åse K.
- Gerdes, Anne-Marie
- Skytte, Anne-Bine
- Jensen, Uffe B.
- Nielsen, Finn C.
- Hansen, Thomas v. O.
- SpringerLink (Online service)
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Paraganglioma and pheochromocytoma upon maternal transmission of SDHDmutations
Emerging Treatments for Advanced/Metastatic Pheochromocytoma and Paraganglioma
The diagnosis and management of pheochromocytoma and paraganglioma during pregnancy
Analysis of SDHAF3 in familial and sporadic pheochromocytoma and paraganglioma
Metabolic implications of hypoxia and pseudohypoxia in pheochromocytoma and paraganglioma
The first Dutch SDHB founder deletion in paraganglioma – pheochromocytoma patients
Current status of functional imaging in neuroblastoma, pheochromocytoma, and paraganglioma disease
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