Detalhe da pesquisa
1.
Screening of 23 candidate genes by next-generation sequencing of patients with permanent congenital hypothyroidism: novel variants in TG, TSHR, DUOX2, FOXE1, and SLC26A7.
J Endocrinol Invest
; 45(4): 773-786, 2022 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-34780050