Publication | Closed Access

Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16

Atrial Septal DefectGenome-wide Association StudyGenetic DisorderGeneticsGenetic EpidemiologyCongenital Heart DefectGenomicsCongenital Heart AnomalySystems BiologyMedicineSusceptibility LocusCardiovascular Genetics