ADGRV1 and Tetralogy of Fallot: Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3 Circ Cardiovasc Genet Circ Cardiovasc Genet 2017 2017 10 10 5 5 https://doi: 10.1007/s00439-015-1623-9 https://doi: 10.1007/s00439-015-1623-9