Molecular analysis of patients with congenital hypothyroidism by iodine defect
Study of mutations in PAX-8 and TSH receptor genes after determination of congenit...
Molecular diagnosis in suspected patients with thyroglobulin and thyroperoxidase d...
Molecular analysis of patients with congenital hipothyroidism by iodine organifica...
Neuropsychomotor development of infants with congenital hypothyroidism
Correlation between cervical uptake values on whole body scan, ultrasound and thyr...