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3. Molecular profiling in primary hyperparathyroidism. Segiet OA; Deska M; Michalski M; Gawrychowski J; Wojnicz R Head Neck; 2015 Feb; 37(2):299-307. PubMed ID: 24595969 [TBL] [Abstract][Full Text] [Related]
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18. Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP). Villablanca A; Calender A; Forsberg L; Höög A; Cheng JD; Petillo D; Bauters C; Kahnoski K; Ebeling T; Salmela P; Richardson AL; Delbridge L; Meyrier A; Proye C; Carpten JD; Teh BT; Robinson BG; Larsson C J Med Genet; 2004 Mar; 41(3):e32. PubMed ID: 14985403 [No Abstract] [Full Text] [Related]
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20. One hundred and seven family members with the rearranged during transfection V804M proto-oncogene mutation presenting with simultaneous medullary and papillary thyroid carcinomas, rare primary hyperparathyroidism, and no pheochromocytomas: is this a new syndrome--MEN 2C? Shifrin AL; Xenachis C; Fay A; Matulewicz TJ; Kuo YH; Vernick JJ Surgery; 2009 Dec; 146(6):998-1005. PubMed ID: 19958926 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]