Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype
Version of Record online: 16 MAY 2011
© 2011 John Wiley & Sons A/S
Volume 81, Issue 2, pages 128–141, February 2012
How to Cite
D'Amours, G., Kibar, Z., Mathonnet, G., Fetni, R., Tihy, F., Désilets, V., Nizard, S., Michaud, J. and Lemyre, E. (2012), Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype. Clinical Genetics, 81: 128–141. doi: 10.1111/j.1399-0004.2011.01687.x
- Issue online: 12 JAN 2012
- Version of Record online: 16 MAY 2011
- Accepted manuscript online: 15 APR 2011 10:32AM EST
- Received 8 February 2011, revised and accepted for publication 11 April 2011
The following Supporting information is available for this article:
Table S1. Cohort description
Additional Supporting information may be found in the online version of this article.
|CGE_1687_sm_suppinfo.pdf||210K||Supporting info item|
|CGE_1687_sm_ts1.xls||42K||Supporting info item|
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