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5. Coincidence of multiple endocrine neoplasia types 1 and 2: mutations in the RET protooncogene and MEN1 tumor suppressor gene in a family presenting with recurrent primary hyperparathyroidism. Frank-Raue K, Rondot S, Hoeppner W, Goretzki P, Raue F, Meng W. J Clin Endocrinol Metab; 2005 Jul; 90(7):4063-7. PubMed ID: 15870131 [Abstract] [Full Text] [Related]
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