Fig. 1From: Enrichment of small pathogenic deletions at chromosome 9p24.3 and 9q34.3 involving DOCK8, KANK1, EHMT1 genes identified by using high-resolution oligonucleotide-single nucleotide polymorphism array analysisThe recurrent small pathogenic small copy number losses from all the chromosomes. The small pathogenic deletions on chromosome 9, involving DOCK8, KANK1, EHMT1 genes constituted a significant proportion (12 %) of casesBack to article page