Fig. 5From: Fraternal twins with Phelan-McDermid syndrome not involving the SHANK3 gene: case report and literature reviewMapping of the 22q13 deletions: our cases (red), one patient described by Palumbo et al. [2017] (purple), nine patients described by Disciglio et al. [2014] (brown), three patients described by Wilson et al. [2008] (green) and one patient from the DECIPHER database (black) in the UCSC Genome Browser (GRCh37/hg19). Our cases’ deletion region is represented by the blue-shadow box (not involving the SHANK3 gene)Back to article page