Detalhe da pesquisa
1.
Congenital Hypothyroidism in Two Sudanese Families Harboring a Novel Iodotyrosine Deiodinase Mutation (IYD R279C).
Thyroid
; 33(2): 261-266, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36633921
2.
Insertion of an Alu Element in Thyroglobulin Gene as a Novel Cause of Congenital Hypothyroidism.
Thyroid
; 30(5): 780-782, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31868128