Fig. 1From: 3p22.1p21.31 microdeletion identifies CCK as Asperger syndrome candidate gene and shows the way for therapeutic strategies in chromosome imbalancesSchematic overview of the deletion of the short arm of chromosome 3 (3p22.1p21.31) depicted using UCSC Genome Browser (Human Feb. 2009 (GRCh37/hg19 assembly), http://genome-euro.ucsc.edu/index.html) showing OMIM (Online Mendelian Inheritance in Man) genes (genes associated with OMIM disorders are shown in green)Back to article page