Source: Journal of pediatric endocrinology & metabolism. Unidade: FM
Subjects: CRIANÇAS, GLÂNDULA TIREOIDE, HIPOTIREOIDISMO, MUTAÇÃO GENÉTICA
ABNT
PERONE, Denise et al. Analysis of the PAX8 gene in 32 children with thyroid dysgenesis and functional characterization of a promoter variant. Journal of pediatric endocrinology & metabolism, v. 29, n. 2, p. 193-201, 2016Tradução . . Disponível em: https://doi.org/10.1515/jpem-2015-0199. Acesso em: 01 nov. 2024.APA
Perone, D., Medeiros-Neto, G., Nogueira, C. R., Chagas, A. J., Dias, V. M. A., Viana, M. F., & Kopp, P. (2016). Analysis of the PAX8 gene in 32 children with thyroid dysgenesis and functional characterization of a promoter variant. Journal of pediatric endocrinology & metabolism, 29( 2), 193-201. doi:10.1515/jpem-2015-0199NLM
Perone D, Medeiros-Neto G, Nogueira CR, Chagas AJ, Dias VMA, Viana MF, Kopp P. Analysis of the PAX8 gene in 32 children with thyroid dysgenesis and functional characterization of a promoter variant [Internet]. Journal of pediatric endocrinology & metabolism. 2016 ; 29( 2): 193-201.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1515/jpem-2015-0199Vancouver
Perone D, Medeiros-Neto G, Nogueira CR, Chagas AJ, Dias VMA, Viana MF, Kopp P. Analysis of the PAX8 gene in 32 children with thyroid dysgenesis and functional characterization of a promoter variant [Internet]. Journal of pediatric endocrinology & metabolism. 2016 ; 29( 2): 193-201.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1515/jpem-2015-0199