Fig. 2From: A novel de novo microdeletion at 17q11.2 adjacent to NF1 gene associated with developmental delay, short stature, microcephaly and dysmorphic featuresSNP array profile showing a deletion on 17q11.2 (a), and schematic representation of 27 Mbp to 31Mbp in 17q11.2 region (b). Blue bars represent genes discussed in this paper. Also shown, the extent of the deletions (in red) observed in reported cases are compared with the presented caseBack to article page