Language delay as first manifestation of congenital hypothyroidism in suspected case of MCT8 mutation

Language delay as first manifestation of congenital hypothyroidism in suspected case of MCT8 mutation (2017)

Authors:
USP affiliated authors: MARTINELLI JUNIOR, CARLOS EDUARDO - FMRP ; CIAMPO, LUIZ ANTONIO DEL - FMRP ; FERRAZ, IVAN SAVIOLI - FMRP ; MACIEL, LEA MARIA ZANINI - FMRP
Unidade: FMRP
Subjects: HIPOTIREOIDISMO; DISTÚRBIOS DA FALA
Language: Inglês
Imprenta:
- Publisher place: Washington
- Date published: 2017
Source:
- Título: Abstracts
Conference titles: International Meeting of Pediatric Endocrinology

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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: 13 mar. 2026.
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 2026 mar. 13 ]
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 2026 mar. 13 ]