共 50 条
- [33] Clinical and molecular genetics of acromegaly: MEN1, Carney complex, McCune-Albright syndrome, familial acromegaly and genetic defects in sporadic tumors [J]. REVIEWS IN ENDOCRINE & METABOLIC DISORDERS, 2008, 9 (01): : 1 - 11
- [34] Rapid mutation screening for HRPT2 and MEN1 mutations associated with familial and sporadic primary hyperparathyroidism [J]. JOURNAL OF MOLECULAR DIAGNOSTICS, 2006, 8 (05): : 559 - 566
- [35] Discovery of MEN1 mutations in familial isolated hyperparathyroidism [J]. Nature Clinical Practice Endocrinology & Metabolism, 2006, 2 (4): : 183 - 184
- [40] Increased MEN1 mRNA expression in sporadic pituitary tumours [J]. CLINICAL ENDOCRINOLOGY, 1999, 50 (06) : 727 - 733