Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 2 (of 2 Records) |
Query Trace: Hereditary Paraganglioma-pheochromocytoma[original query] |
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Isocitrate dehydrogenase mutations are rare in pheochromocytomas and paragangliomas. The Journal of clinical endocrinology and metabolism 2010 Mar 95 (3): 1274-8. Gaal José, Burnichon Nelly, Korpershoek Esther, Roncelin Isabelle, Bertherat Jérôme, Plouin Pierre-François, de Krijger Ronald R, Gimenez-Roqueplo Anne-Paule, Dinjens Winand N |
The utility of SDHB and FH immunohistochemistry in patients evaluated for hereditary paraganglioma-pheochromocytoma syndromes. Human pathology 2018 01 71 47-54. Udager Aaron M, Magers Martin J, Goerke Dayna M, Vinco Michelle L, Siddiqui Javed, Cao Xuhong, Lucas David R, Myers Jeffrey L, Chinnaiyan Arul M, McHugh Jonathan B, Giordano Thomas J, Else Tobias, Mehra Roh |
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