Browsing by Subject "ENDOCRINE NEOPLASIA TYPE-1"

Now showing items 1-1 of 1

    • Novel intronic mutation of MEN1 gene causing familial isolated primary hyperparathyroidism 
      Carrasco, Carmen A.; González, Alexis A.; Carvajal, Cristián A.; Campusano, Claudia; Oestreicher, Eveline; Artega, Eugenio; Wohllk González, Nelson; Fardella, Carlos E. (ENDOCRINE SOC, 2004-08)
      Primary hyperparathyroidism may occur as part of hereditary syndromes, including multiple endocrine neoplasia types 1 and 2A (MEN1 and MEN2A), hyperparathyroidism-jaw tumor syndrome, and the familial isolated hyperparathyroidism ...