Absence seizures with intellectual disability as a phenotype of the 15q13.3 microdeletion syndrome
Version of Record online: 2 NOV 2011
Wiley Periodicals, Inc. © 2011 International League Against Epilepsy
Volume 52, Issue 12, pages e194–e198, December 2011
How to Cite
Muhle, H., Mefford, H. C., Obermeier, T., von Spiczak, S., Eichler, E. E., Stephani, U., Sander, T. and Helbig, I. (2011), Absence seizures with intellectual disability as a phenotype of the 15q13.3 microdeletion syndrome. Epilepsia, 52: e194–e198. doi: 10.1111/j.1528-1167.2011.03301.x
- Issue online: 2 DEC 2011
- Version of Record online: 2 NOV 2011
- Accepted September 6, 2011; Early View publication November 2, 2011.
Figure S1. Array-CGH in probands with identified 15q13 microdeletions.
Figure S2. MRI scans of patient 4 demonstrating a small right occipital subependymal periventricular heterotopia marked by an arrow.
Table S1. Phenotypes of probands screened for 15q13.3 microdeletions.
Table S2. Clinical and genetic data in 15q13.3 microdeletion carriers.
|EPI_3301_sm_FigS1.tif||1137K||Supporting info item|
|EPI_3301_sm_FigS2.tif||1438K||Supporting info item|
|EPI_3301_sm_supplementaryLegends.doc||13K||Supporting info item|
|EPI_3301_sm_TableS1.doc||64K||Supporting info item|
|EPI_3301_sm_TableS2.doc||52K||Supporting info item|
Please note: Wiley Blackwell is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.