Use of Next Generation Sequencing to study karyotypes with different number of X c...
Identifying Copy Number Variations (CNVs) and Epigenetic Changes in Patients with ...
Investigation of copy number variation by SNP array in congenital defects with com...
SNP Arrays data bank analysis of patients with malformations and delay in neuropsy...
Analysis of cell-free DNA sequencing data in order to infer the fetal fraction of ...
Searching for mutations associated with focal cortical dysplasia using genomic str...
Alterations of DNA segments copy number and evaluation of the miRNAs expression pa...