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Fig. 2 | BMC Medical Genomics

Fig. 2

From: 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 anomalies

Fig. 2

Array-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) enhancers

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BMC Medical Genomics

ISSN: 1755-8794

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