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This page is a summary of: 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, Circulation Cardiovascular Genetics, October 2017, Wolters Kluwer Health,
DOI: 10.1161/circgenetics.116.001690.
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