These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
10. Germline mutations of the MEN1 gene in Korean families with multiple endocrine neoplasia type 1 (MEN1) or MEN1-related disorders. Park JH; Kim IJ; Kang HC; Lee SH; Shin Y; Kim KH; Lim SB; Kang SB; Lee K; Kim SY; Lee MS; Lee MK; Park JH; Moon SD; Park JG Clin Genet; 2003 Jul; 64(1):48-53. PubMed ID: 12791038 [TBL] [Abstract][Full Text] [Related]
11. Absence of germ-line mutations of the multiple endocrine neoplasia type 1 (MEN1) gene in familial pituitary adenoma in contrast to MEN1 in Japanese. Tanaka C; Yoshimoto K; Yamada S; Nishioka H; Ii S; Moritani M; Yamaoka T; Itakura M J Clin Endocrinol Metab; 1998 Mar; 83(3):960-5. PubMed ID: 9506756 [TBL] [Abstract][Full Text] [Related]
13. A novel mutation of the MEN1 gene in a Japanese kindred with familial isolated primary hyperparathyroidism. Honda M; Tsukada T; Tanaka H; Maruyama K; Yamaguchi K; Obara T; Yamaji T; Ishibashi M Eur J Endocrinol; 2000 Feb; 142(2):138-43. PubMed ID: 10664521 [TBL] [Abstract][Full Text] [Related]
14. Multiple endocrine neoplasia type 1 (MEN1). Thakker RV Best Pract Res Clin Endocrinol Metab; 2010 Jun; 24(3):355-70. PubMed ID: 20833329 [TBL] [Abstract][Full Text] [Related]
15. Multiple endocrine neoplasia type 1 (MEN1): clinical heterogeneity in a large family with a nonsense mutation in the MEN1 gene (Trp471Stop). Valdés N; Pérez de Nanclares G; Alvarez V; Castaño L; Díaz-Cadórniga F; Aller J; Coto E Clin Endocrinol (Oxf); 1999 Mar; 50(3):309-13. PubMed ID: 10435055 [TBL] [Abstract][Full Text] [Related]
16. Familial isolated hyperparathyroidism is rarely caused by germline mutation in HRPT2, the gene for the hyperparathyroidism-jaw tumor syndrome. Simonds WF; Robbins CM; Agarwal SK; Hendy GN; Carpten JD; Marx SJ J Clin Endocrinol Metab; 2004 Jan; 89(1):96-102. PubMed ID: 14715834 [TBL] [Abstract][Full Text] [Related]
17. Frequency of somatic MEN1 gene mutations in monoclonal parathyroid tumours of patients with primary hyperparathyroidism. Miedlich S; Krohn K; Lamesch P; Müller A; Paschke R Eur J Endocrinol; 2000 Jul; 143(1):47-54. PubMed ID: 10870030 [TBL] [Abstract][Full Text] [Related]
18. Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism. Teh BT; Kytölä S; Farnebo F; Bergman L; Wong FK; Weber G; Hayward N; Larsson C; Skogseid B; Beckers A; Phelan C; Edwards M; Epstein M; Alford F; Hurley D; Grimmond S; Silins G; Walters M; Stewart C; Cardinal J; Khodaei S; Parente F; Tranebjaerg L; Jorde R; Salmela P J Clin Endocrinol Metab; 1998 Aug; 83(8):2621-6. PubMed ID: 9709921 [TBL] [Abstract][Full Text] [Related]
20. Familial isolated primary hyperparathyroidism/hyperparathyroidism-jaw tumour syndrome caused by germline gross deletion or point mutations of CDC73 gene in Chinese. Kong J; Wang O; Nie M; Shi J; Hu Y; Jiang Y; Li M; Xia W; Meng X; Xing X Clin Endocrinol (Oxf); 2014 Aug; 81(2):222-30. PubMed ID: 24716902 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]