A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutation

MLA

Meyer Knobel, et al. “A Molecular Analysis and Long-Term Follow-up of Two Siblings with Severe Congenital Hypothyroidism Carrying the IVS30+1G>T Intronic Thyroglobulin Mutation.” Arquivos Brasileiros de Endocrinologia & Metabologia, vol. 52, Nov. 2008, pp. 1337–44. EBSCOhost, https://doi.org/10.1590/s0004-27302008000800022.

APA

Meyer Knobel, Viviane Pardo, Ileana G.S. Rubio, Ana Luiza Galrao, Geraldo Medeiros-Neto, Simone A. Gomes, Cristina Takami Kanamura, Rosalinda Camargo, Marcelo Alves Ferreira, & Roberta F. Possato. (2008). A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutation. Arquivos Brasileiros de Endocrinologia & Metabologia, 52, 1337–1344. https://doi.org/10.1590/s0004-27302008000800022

Chicago

Meyer Knobel, Viviane Pardo, Ileana G.S. Rubio, Ana Luiza Galrao, Geraldo Medeiros-Neto, Simone A. Gomes, Cristina Takami Kanamura, Rosalinda Camargo, Marcelo Alves Ferreira, and Roberta F. Possato. 2008. “A Molecular Analysis and Long-Term Follow-up of Two Siblings with Severe Congenital Hypothyroidism Carrying the IVS30+1G>T Intronic Thyroglobulin Mutation.” Arquivos Brasileiros de Endocrinologia & Metabologia 52 (November): 1337–44. doi:10.1590/s0004-27302008000800022.