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

Internet

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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