Molecular analysis of patients with congenital hypothyroidism by iodine defect
Molecular diagnosis in suspected patients with thyroglobulin and thyroperoxidase d...
Study of mutations in PAX-8 and TSH receptor genes after determination of congenit...
Thyroid dysgenesis: screening and functional analyses of mutations of the candidat...
Congenital hypothyroidism due to thyroid disgenesis: whole exome investigation of ...
Functional analyses of novel nucleotides variations in the CYP21A2 gene identified...