Fonte: Abstracts. Nome do evento: International Meeting of Pediatric Endocrinology. Unidade: FMRP
Assuntos: HIPOTIREOIDISMO, DISTÚRBIOS DA FALA
ABNT
ARAÚJO, Aiana A. et al. Language delay as first manifestation of congenital hypothyroidism in suspected case of MCT8 mutation. 2017, Anais.. Washington: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2017. . Acesso em: 27 jun. 2024.APA
Araújo, A. A., Siena, T. A., Paula, M. T. S. de, Maciel, L. M. Z., Ferraz, I. S., Del Ciampo, L. A., & Martinelli Júnior, C. E. (2017). Language delay as first manifestation of congenital hypothyroidism in suspected case of MCT8 mutation. In Abstracts. Washington: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.NLM
Araújo AA, Siena TA, Paula MTS de, Maciel LMZ, Ferraz IS, Del Ciampo LA, Martinelli Júnior CE. Language delay as first manifestation of congenital hypothyroidism in suspected case of MCT8 mutation. Abstracts. 2017 ;[citado 2024 jun. 27 ]Vancouver
Araújo AA, Siena TA, Paula MTS de, Maciel LMZ, Ferraz IS, Del Ciampo LA, Martinelli Júnior CE. Language delay as first manifestation of congenital hypothyroidism in suspected case of MCT8 mutation. Abstracts. 2017 ;[citado 2024 jun. 27 ]