An atypical deletion of the Williams–Beuren syndrome interval implicates genes associated with defective visuospatial processing and autism
L. Edelmann, A. Prosnitz, S. Pardo, J. Bhatt, N. Cohen, T. Lauriat, L. Ouchanov, P. J González, E. R Manghi, P. Bondy, M. Esquivel, S. Monge, M. F Delgado, A. Splendore, U. Francke, B. K Burton, and L A. McInnes
Supplementary Data Figure 1. Gene expression analysis in transformed lymphocytes
Chart displaying quantitative RT-PCR gene expression values from transformed lymphocytes in Case 41A and both parents, 41B and 41C, for the genes GTF2I, YWHAG and GTF2IRD1 and HIP1. For each gene, relative expression values were normalized to the mean of 41B and 41C.
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