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Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartomas and cystic kidney disease: linkage to 1q21-q32 and loss of the wild type allele in renal hamartomas.
Teh BT, Farnebo F, Kristoffersson U, Sundelin B, Cardinal J, Axelson R, Yap A, Epstein M, Heath H 3rd, Cameron D, Larsson C. Teh BT, et al. Among authors: cardinal j. J Clin Endocrinol Metab. 1996 Dec;81(12):4204-11. doi: 10.1210/jcem.81.12.8954016. J Clin Endocrinol Metab. 1996. PMID: 8954016
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, et al. Teh BT, et al. Among authors: cardinal j. J Clin Endocrinol Metab. 1998 Aug;83(8):2621-6. doi: 10.1210/jcem.83.8.5059. J Clin Endocrinol Metab. 1998. PMID: 9709921 Free article.
164 results