Activating FGFR1 Mutations in Sporadic Pheochromocytomas

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1432-2323

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Activating FGFR1 Mutations in Sporadic Pheochromocytomas ; volume:42 ; number:2 ; day:20 ; month:11 ; year:2017 ; pages:482-489 ; date:2.2018
World journal of surgery ; 42, Heft 2 (20.11.2017), 482-489, 2.2018

Creator: Welander, Jenny

Contributor: Łysiak, Małgorzata
Brauckhoff, Michael
Brunaud, Laurent
Söderkvist, Peter
Gimm, Oliver
SpringerLink (Online service)

DOI: 10.1007/s00268-017-4320-0

URN: urn:nbn:de:1111-2018030531

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:46 AM CEST

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Welander, Jenny
Łysiak, Małgorzata
Brauckhoff, Michael
Brunaud, Laurent
Söderkvist, Peter
Gimm, Oliver
SpringerLink (Online service)

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Activating FGFR1 Mutations in Sporadic Pheochromocytomas

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Other Objects (12)

Sporadic multiple meningiomas harbor distinct driver mutations

Kallmann syndrome with FGFR1 and KAL1 mutations detected during fetal life

Three novel F8 mutations in sporadic haemophilia A cases

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Sporadic and Familial Acute Myeloid Leukemia with CEBPA Mutations

Trans-activating mutations of the pseudokinase ERBB3

Sporadic PCDH18 somatic mutations in EpCAM-positive hepatocellular carcinoma

ATM gene mutations in sporadic breast cancer patients from Brazil

CDC73 gene mutations in sporadic ossifying fibroma of the jaws

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Mutation spectrum of Kallmann syndrome: identification of five novel mutations across ANOS1 and FGFR1

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Three novel F8 mutations in sporadic haemophilia A cases

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Sporadic and Familial Acute Myeloid Leukemia with CEBPA Mutations

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Kallmann syndrome with FGFR1 and KAL1 mutations detected during fetal life

Three novel F8 mutations in sporadic haemophilia A cases

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Sporadic and Familial Acute Myeloid Leukemia with CEBPA Mutations

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FGF2/FGFR1 regulates autophagy in FGFR1-amplified non-small cell lung cancer cells

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