Figure 5From: A novel custom high density-comparative genomic hybridization array detects common rearrangements as well as deep intronic mutations in dystrophinopathiesGenomic configuration in patient 6. a) Schemes of the inverted genomic region including exon 45 in patient 6 and primers position. PCR amplification for the detection of inversion breakpoints was carried out using two forward primers (black arrows) and two reverse primers (grey arrows) surrounding the breakpoint regions; b) PCR results in patient 6: Lane 1 molecular weight marker VI, Lane 2: proximal breakpoint (int44/int45(inv), Lane 3: distal breakpoint (int44(inv)/int45).Back to article page