Fig. 2From: A case report of familial 4q13.3 microdeletion in three individuals with syndromic intellectual disability1.56 Mb deletion, arr[hg19] 4q13.3(72,647,749_74,208,199)×1 detected by SNP oligonucleotide microarray analysis and a schematic view of the genes. Horizontal white bars below represent deletionsBack to article page