Figure 3From: Isochromosome 13 in a patient with childhood-onset schizophrenia, ADHD, and motor tic disorderChromosome 22 Affymetrix Whole-Genome Human SNP 6.0 analysis. The 1.5 Mb region of chromosome 22 associated with 22q11.2 Deletion Syndrome in schizophrenia [85] is noted by a box. The patient and her mother both contain a small duplication at the centromeric end of the 22q11.2 deletion syndrome region, but neither has a deletion.Back to article page