Pheochromocytoma and Paraganglioma
Author:
Publisher
Elsevier BV
Subject
Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism
Link
http://aace.metapress.com/index/Q70RV8243162R90H.pdf
Reference38 articles.
1. Pheochromocytoma and functional paraganglioma syndrome: no longer the 10% tumor;Elder;J Surg Oncol,2005
2. Pheochromocytoma and paraganglioma: diagnosis, genetics, management, and treatment;Martucci;Curr Probl Cancer,2014
3. Germ-line PHD1 and PHD2 mutations detected in patients with pheochromocytoma/paraganglioma-polycythemia;Yang;J Mol Med (Berl),2015
4. Wholeexome sequencing identifies somatic ATRX mutations in pheochromocytomas and paragangliomas;Fishbein;Nat Commun,2015
5. Whole-exome sequencing identifies MDH2 as a new familial paraganglioma gene;Cascón;J Natl Cancer Inst,2015
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