Author:
Eijkelenkamp Karin,Osinga Thamara E.,de Jong Mirjam M.,Sluiter Wim J.,Dullaart Robin P. F.,Links Thera P.,Kerstens Michiel N.,van der Horst-Schrivers Anouk N. A.
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Genetics (clinical),Oncology,Genetics
Reference23 articles.
1. Pillai S, Gopalan V, Smith RA et al (2016) Updates on the genetics and the clinical impacts on phaeochromocytoma and paraganglioma in the new era. Crit Rev Oncol Hematol 100:190–208
2. Astuti D, Latif F, Dallol A et al (2001) Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma. Am J Hum Genet 69(1):49–54
3. Dutch guideline for detecting hereditary tumors 2010. https://www.stoet.nl
4. Kirmani S, Young WF (2014) Hereditary paraganglioma-pheochromocytoma syndrome. In: Pagon RA, Adam MP, Ardinger HH et al (eds) GeneReviews. University of Washington, Seattle
5. Taieb D, Kaliski A, Boedeker CC et al (2014) Current approaches and recent developments in the management of head and neck paragangliomas. Endocr Rev 35(5):795–819
Cited by
31 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献