Arq Bras Endocrinol Metab 2012;56(2):152
Which is the role for inherited TR? mutation in human thyroid carcinogenesis?
DOI: 10.1590/S0004-27302012000200010
Flow diagram of patient exclusion criteria for SNMTC and FNMTC groups.
Weinert LS, Ceolin L, Romitti M, Camargo EG, Maia AL. Which is the role for inherited TR? mutation in human thyroid carcinogenesis?. Arq Bras Endocrinol Metab 2012;56(2):152.
Weinert, Letícia Schwerz; Ceolin, Lucieli; Romitti, Mírian; Camargo, Eduardo Guimarães; Maia, Ana Luiza. Which is the role for inherited TR? mutation in human thyroid carcinogenesis?. Arq Bras Endocrinol Metab, v. 56, n. 2, p. 152-152, Mar. 2012.
Weinert, L. S., Ceolin, L., Romitti, M., Camargo, E. G., & Maia, A. L. (2012). Which is the role for inherited TR? mutation in human thyroid carcinogenesis?. Arq Bras Endocrinol Metab, 56(2), 152-152.
Weinert, Letícia Schwerz and Ceolin, Lucieli and Romitti, Mírian and Camargo, Eduardo Guimarães and Maia, Ana Luiza. Which is the role for inherited TR? mutation in human thyroid carcinogenesis?. Arq Bras Endocrinol Metab [online]. 2012, vol. 56, n. 2, [cited 2026-03-07], pp.152-152. Available from: <https://www.aem-sbem.com/article/which-is-the-role-for-inherited-tr-mutation-in-human-thyroid-carcinogenesis/>. ISSN 2359-3997.