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Mutation screening in the genes PAX-8, NKX2-5, TSH-R, HES-1 in cohort of 63 Brazilian children with thyroid dysgenesis

OBJECTIVE: To evaluate the candidate genes PAX-8, NKX2-5, TSH-R and HES-1 in 63 confirmed cases of thyroid dysgenesis. SUBJECTS AND METHODS: Characterization of patients with congenital hypothyroidism into specific subtypes of thyroid dysgenesis with hormone levels (TT4 and TSH), thyroid ultrasound...

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Detalles Bibliográficos
Autores principales:	Cerqueira, Taíse Lima de Oliveira, Ramos, Yanne Rocha, Strappa, Giorgia Bruna, de Jesus, Mariana Souza, Santos, Jailciele Gonzaga, Sousa, Camila, Carvalho, Gildásio, Fernandes, Vladimir, Boa-Sorte, Ney, Amorim, Tatiana, Silva, Thiago Magalhães, Ladeia, Ana Marice Teixeira, Acosta, Angelina Xavier, Ramos, Helton Estrela
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Sociedade Brasileira de Endocrinologia e Metabologia 2018
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10118737/ https://www.ncbi.nlm.nih.gov/pubmed/30304112 http://dx.doi.org/10.20945/2359-3997000000065

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