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7. Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas. Benn DE; Croxson MS; Tucker K; Bambach CP; Richardson AL; Delbridge L; Pullan PT; Hammond J; Marsh DJ; Robinson BG Oncogene; 2003 Mar; 22(9):1358-64. PubMed ID: 12618761 [TBL] [Abstract][Full Text] [Related]
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9. Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma. Astuti D; Latif F; Dallol A; Dahia PL; Douglas F; George E; Sköldberg F; Husebye ES; Eng C; Maher ER Am J Hum Genet; 2001 Jul; 69(1):49-54. PubMed ID: 11404820 [TBL] [Abstract][Full Text] [Related]
10. A Novel SDHB IVS2-2A>C Mutation Is Responsible for Hereditary Pheochromocytoma/Paraganglioma Syndrome. Yamanaka M; Shiga K; Fujiwara S; Mizuguchi Y; Yasuda S; Ishizawa K; Saiki Y; Higashi K; Ogawa T; Kimura N; Horii A Tohoku J Exp Med; 2018 Jun; 245(2):99-105. PubMed ID: 29925701 [TBL] [Abstract][Full Text] [Related]
11. SDHB-related pheochromocytoma and paraganglioma penetrance and genotype-phenotype correlations. Jochmanova I; Wolf KI; King KS; Nambuba J; Wesley R; Martucci V; Raygada M; Adams KT; Prodanov T; Fojo AT; Lazurova I; Pacak K J Cancer Res Clin Oncol; 2017 Aug; 143(8):1421-1435. PubMed ID: 28374168 [TBL] [Abstract][Full Text] [Related]
12. Low penetrance of paraganglioma and pheochromocytoma in an extended kindred with a germline SDHB exon 3 deletion. Rijken JA; Niemeijer ND; Corssmit EP; Jonker MA; Leemans CR; Menko FH; Hensen EF Clin Genet; 2016 Jan; 89(1):128-32. PubMed ID: 25827221 [TBL] [Abstract][Full Text] [Related]
13. High prevalence of SDHB mutations in head and neck paraganglioma in Belgium. Persu A; Hamoir M; Grégoire V; Garin P; Duvivier E; Reychler H; Chantrain G; Mortier G; Mourad M; Maiter D; Vikkula M J Hypertens; 2008 Jul; 26(7):1395-401. PubMed ID: 18551016 [TBL] [Abstract][Full Text] [Related]
14. A Patient with an Extra-adrenal Pheochromocytoma and Germ-line SDHB Mutation Accompanied by an Atypical Meningioma. Shiwa T; Oki K; Yoneda M; Arihiro K; Ohno H; Kishimoto R; Kohno N Intern Med; 2015; 54(18):2355-60. PubMed ID: 26370861 [TBL] [Abstract][Full Text] [Related]
15. [Familial paraganglioma syndrome: phenotype and relevance of a new SDHB mutation]. Díaz-Soto G; Serrano Morte A; Rodríguez Martín C; García-Talavera P; Abril CM; Puig-Domingo M Med Clin (Barc); 2013 May; 140(10):453-7. PubMed ID: 23434467 [TBL] [Abstract][Full Text] [Related]
16. Analysis of SDHAF3 in familial and sporadic pheochromocytoma and paraganglioma. Dwight T; Na U; Kim E; Zhu Y; Richardson AL; Robinson BG; Tucker KM; Gill AJ; Benn DE; Clifton-Bligh RJ; Winge DR BMC Cancer; 2017 Jul; 17(1):497. PubMed ID: 28738844 [TBL] [Abstract][Full Text] [Related]