These authors contributed equally to this paper.
Clinical application of 2.7M Cytogenetics array for CNV detection in subjects with idiopathic autism and/or intellectual disability
Version of Record online: 9 APR 2012
© 2012 John Wiley & Sons A/S. Published by Blackwell Publishing Ltd
Volume 83, Issue 2, pages 145–154, February 2013
How to Cite
Qiao, Y., Tyson, C., Hrynchak, M., Lopez-Rangel, E., Hildebrand, J., Martell, S., Fawcett, C., Kasmara, L., Calli, K., Harvard, C., Liu, X., Holden, J., Lewis, S. and Rajcan-Separovic, E. (2013), Clinical application of 2.7M Cytogenetics array for CNV detection in subjects with idiopathic autism and/or intellectual disability. Clinical Genetics, 83: 145–154. doi: 10.1111/j.1399-0004.2012.01860.x
- Issue online: 7 JAN 2013
- Version of Record online: 9 APR 2012
- Accepted manuscript online: 27 FEB 2012 09:06AM EST
- Received 15 November 2011, revised and accepted for publication 21 February 2012
The following Supporting information is available for this article:
Table S1. Thirty cases with Affymetrix 2.7M array results in validation study.
Table S2. Most common copy number variations found in Cyto2.7M array among 82 cases (with size >10 kb and frequency >10%).
Additional Supporting information may be found in the online version of this article.
|CGE_1860_sm_ts1.doc||77K||Supporting info item|
|CGE_1860_sm_ts2.doc||24K||Supporting info item|
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