Analysis of primary skin fibroblasts of 8 Williams-Beuren Syndrome (WBS) and 9 control Caucasian females aged 3 to 8 years. WBS is a neurodevelopmental disorder associated with a microdeletion within the 7q11.23 chromosomal band. Results provide insight into the molecular basis of the WBS phenotype.
GPL570:
[HG-U133_Plus_2] Affymetrix Human Genome U133 Plus 2.0 Array
Citation:
Henrichsen CN, Csárdi G, Zabot MT, Fusco C et al. Using transcription modules to identify expression clusters perturbed in Williams-Beuren syndrome. PLoS Comput Biol 2011 Jan 20;7(1):e1001054. PMID: 21304579