Conflict of interest: none.
5q31.3 Microdeletion syndrome: Clinical and molecular characterization of two further cases
Article first published online: 15 AUG 2013
Copyright © 2013 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 161, Issue 10, pages 2604–2608, October 2013
How to Cite
2013. 5q31.3 Microdeletion syndrome: Clinical and molecular characterization of two further cases. Am J Med Genet Part A 161A:2604–2608., , , , , , .
- Issue published online: 17 SEP 2013
- Article first published online: 15 AUG 2013
- Manuscript Accepted: 16 MAY 2013
- Manuscript Received: 25 FEB 2013
Additional supporting information may be found in the online version of this article at the publisher's web-site.
|ajma36108-sm-0001-SupFig-S1.pptx||637K||FIG. S1. Expanded view of the 5q31.3 deleted region in Patient 1 obtained using the Illumina Human CytoSNP-12 v2.1 platform, demonstrating no evidence of the distal duplication originally observed using Affymetrix Genome-Wide SNP Array 6.0, with both the copy number (logR) and the genotyping data being normal in the highlighted region.|
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