STUDY: The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome

Study Description

Here we aimed to contribute to the description of the genetic architecture of Congenital heart defect (CHD) in Down syndrome (DS), and report the... Show More

Study Accession Alternative Stable ID type
EGAS00000000129 Genotype


Data provider(s)

Who archives the data?

European Genome-phenome Archive