Fig. 2From: Co-occurrence of genomic imbalances on Xp22.1 in the SHOX region and 15q25.2 in a girl with short stature, precocious puberty, urogenital malformations and bone anomaliesArray-CGH profile performed with a high resolution array containing 8072 probes within the PAR1 region. The two gains (blue bars) flanking the SHOX coding region from Xp22.33 192,136–494,191 × 3 and 686,753–1453,835 × 3 (NCBI build 37, hg 19) respectively, are shown. The unbalances include the CNE elements corresponding to the upstream (CNE1–3) and downstream (CNE1–8) enhancersBack to article page