Harmonization of whole genome sequencing data for gene-environment interaction ana...
Characterization of INDELs and small CNVs in patients with autism spectrum disorder
Identification of copy number variations (CNVs) in a cohort of children and adoles...
Impact of genetic variants on genomic stability and their effects on the phenotype
Systematic approach and diagnosis of 46, XY differences of sex development: molecu...
Multi-user equipment approved in grant 2019/21644-0: SeqStudio" Genetic Analyzer S...
SNP Arrays data bank analysis of patients with malformations and delay in neuropsy...