Detalhe da pesquisa
1.
Mutational screening of the TPO and DUOX2 genes in Argentinian children with congenital hypothyroidism due to thyroid dyshormonogenesis.
Endocrine
; 77(1): 86-101, 2022 06.
Artigo
Inglês
| MEDLINE | ID: mdl-35507000
2.
Molecular analysis of thyroglobulin mutations found in patients with goiter and hypothyroidism.
Mol Cell Endocrinol
; 473: 1-16, 2018 09 15.
Artigo
Inglês
| MEDLINE | ID: mdl-29275168
3.
Programa de pesquisa neonatal de hipotiroidismo congénito de la provincia de Buenos Aires: 1.377.455 niños evaluados en diez años de experiencia / Newborn screening for congenital hypothyroidism in the province of Buenos Aires. Ten years experience in 1.377.455 evaluated children
Arch. pediatr. Urug
; 80(1): 43-50, 2009. tab
Artigo
Espanhol
| LILACS | ID: lil-537894