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.
| Image |  |
|---|---|
| Description | scientific article published on October 2017 |
| Author/s |
author: Christopher L Campbell Joris R Vermeesch Maude Schneider Bruno Dallapiccola Stephan Eliez Donna M McDonald-McGinn Carrie E Bearden Wendy R Kates Elaine Zackai Elizabeth Goldmuntz |
| Publication date | October 1, 2017 |
| Language | |
| Country of origin | |
| Wikipedia link | |
| Copyright status | |
| Missing/wrong data? | Edit Wikidata item |