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.
Novel DIO1 Gene Mutation Acting as Phenotype Modifier for Novel Compound Heterozygous TPO Gene Mutations Causing Congenital Hypothyroidism.
Thyroid
; 31(10): 1589-1591, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34128397