The Interstitial Duplication 15q11.2-q13 Syndrome Includes Autism, Mild Facial Anomalies and a Characteristic EEG Signature
Article first published online: 14 MAR 2013
© 2013 International Society for Autism Research, Wiley Periodicals, Inc.
Volume 6, Issue 4, pages 268–279, August 2013
How to Cite
Urraca, N., Cleary, J., Brewer, V., Pivnick, E. K., McVicar, K., Thibert, R. L., Schanen, N. C., Esmer, C., Lamport, D. and Reiter, L. T. (2013), The Interstitial Duplication 15q11.2-q13 Syndrome Includes Autism, Mild Facial Anomalies and a Characteristic EEG Signature. Autism Res, 6: 268–279. doi: 10.1002/aur.1284
- Issue published online: 14 AUG 2013
- Article first published online: 14 MAR 2013
- Manuscript Accepted: 15 FEB 2013
- Manuscript Received: 31 AUG 2012
- Herbert and Mary Shainberg Neuroscience Fund
- Le Bonheur Children's Foundation
Figure S1. Online resource. (A) Proximal and (B) distal breakpoints for int dup (15) subjects. University California Santa Cruz tracks being used are chromosome band, segmental duplications, mapability, HapMap single nucleotide polymorphisms (SNPs) and RefSeq Genes. Note the decrease in both mapability and the number of SNPs in regions covered by the segmental duplications. These duplications are located at the breakpoint boundaries for the duplications. In some cases, a single SNP may define the end of the duplication breakpoint, making the accurate mapping of duplication ends quite difficult and somewhat inaccurate within this region.
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