Methylation pattern and HES1, Wnt5a and RET gene expressions in familial and spora...
NEXT GENERATION SEQUENCING FOR DETECTION OF MUTATIONS IN THYROID HURTHLE CELL CARC...
Genomic region 14q32 and thyroid cancer: biological role and clinical implication
RET p.G548V mutation identified in sporadic and hereditary pheochromocytomas: a st...
Functional characterization of BRAFV600E and RET/PTC double mutation and methylati...
Investigation of molecular markers for the diagnosis of MEN 2 through metabolic pr...