Genomic screening in Li-Fraumeni and Li-Fraumeni like families with unknown causes
Analysis of copy number variation (CNV) in pacientes of a family with men 2A and P...
Evaluation of genomic copy number variation of genes that predispose patients with...
Investigation of the molecular basis of familial non-medullary thyroid cancer.
Investigation of genetic factors on etiology of familial melanoma syndrome: evalua...