Molecular analysis of patients with congenital hypothyroidism by iodine defect
Molecular analysis of patients with congenital hipothyroidism by iodine organifica...
Molecular studies in patients with sensorineural deafness and enlarged vestibular ...
Functional characterization of BRAFV600E and RET/PTC double mutation and methylati...
Study of mutations in PAX-8 and TSH receptor genes after determination of congenit...
Characterization of the genetic mechanisms leading to immune evasion in the tumor ...