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Full record GDS3830

Williams-Beuren Syndrome: fibroblast cell lines

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.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 5 age, 2 disease state sets
Platform:
GPL570
Series:
GSE16715
17 Samples
Download data: CEL

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