1. Arbogast, Thomas, Raveau, Matthieu, Chevalier, Claire, Duchon, Arnaud, Herault, Yann. 2015. Deletion of the App-Runx1 region in mice models human partial monosomy 21. In Disease models & mechanisms, 8, 623-34. doi:10.1242/dmm.017814. https://pubmed.ncbi.nlm.nih.gov/26035870/
2. Moon, S, Hwang, M Y, Jang, H B, Song, J, Kim, B-J. 2017. Whole-exome sequencing study reveals common copy number variants in protocadherin genes associated with childhood obesity in Koreans. In International journal of obesity (2005), 41, 660-663. doi:10.1038/ijo.2017.12. https://pubmed.ncbi.nlm.nih.gov/28100915/