Figure 3From: Novel association of severe neonatal encephalopathy and Hirschsprung disease in a male with a duplication at the Xq28 region Schematic representation of the genomic region at Xq28 involved in the duplication in our patient. The regions covered by each of the MLPA sets of probes (P245, P015 and P049) are indicated. The refinement of the region using the Genome wide human SNP 6.0 array of Affymetrix is also shown.Back to article page