HuGE Literature Finder
Records 1-4
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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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Genetics of Apparently Sporadic Pheochromocytoma and Paraganglioma in a Chinese Population.
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme 2015 Aug . Lee C H, Cheung C Y Y, Chow W S, Woo Y C, Yeung C Y, Lang B H H, Fong C H Y, Kwok K H M, Chen S P L, Mak C M, Tan K C B, Lam K S |
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Germline mutations in FH confer predisposition to malignant pheochromocytomas and paragangliomas.
Human molecular genetics 2014 May 23 (9): 2440-6. Castro-Vega Luis Jaime, Buffet Alexandre, De Cubas Aguirre A, Cascón Alberto, Menara Mélanie, Khalifa Emmanuel, Amar Laurence, Azriel Sharona, Bourdeau Isabelle, Chabre Olivier, Currás-Freixes Maria, Franco-Vidal Valérie, Guillaud-Bataille Marine, Simian Christophe, Morin Aurélie, Letón Rocío, Gómez-Graña Alvaro, Pollard Patrick J, Rustin Pierre, Robledo Mercedes, Favier Judith, Gimenez-Roqueplo Anne-Pau |
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Germline SDHB mutations and familial renal cell carcinoma.
Journal of the National Cancer Institute 2008 Sep 100 (17): 1260-2. Ricketts Christopher, Woodward Emma R, Killick Pip, Morris Mark R, Astuti Dewi, Latif Farida, Maher Eamonn |
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- Page last updated:Sep 16, 2021
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