Refining the phenotype associated with MEF2C haploinsufficiency
Article first published online: 27 FEB 2010
© 2010 John Wiley & Sons A/S
Volume 78, Issue 5, pages 471–477, November 2010
How to Cite
Novara, F., Beri, S., Giorda, R., Ortibus, E., Nageshappa, S., Darra, F., Dalla Bernardina, B., Zuffardi, O. and Van Esch, H. (2010), Refining the phenotype associated with MEF2C haploinsufficiency. Clinical Genetics, 78: 471–477. doi: 10.1111/j.1399-0004.2010.01413.x
- Issue published online: 27 FEB 2010
- Article first published online: 27 FEB 2010
- Received 6 November 2009, revised and accepted for publication 22 February 2010
The following Supporting information is available for this article:
Table S1. Cloning of the deletion breakpoints in patients 1 and 2.
Additional Supporting information may be found in the online version of this article.
|CGE_1413_sm_Table1.doc||33K||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.