Communicated by Ravi Savarirayan
Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic features†
Article first published online: 12 MAR 2012
© 2012 Wiley Periodicals, Inc.
Special Issue: Focus on the NIH Undiagnosed Diseases Program
Volume 33, Issue 4, pages 728–740, April 2012
How to Cite
Lamb, A. N., Rosenfeld, J. A., Neill, N. J., Talkowski, M. E., Blumenthal, I., Girirajan, S., Keelean-Fuller, D., Fan, Z., Pouncey, J., Stevens, C., Mackay-Loder, L., Terespolsky, D., Bader, P. I., Rosenbaum, K., Vallee, S. E., Moeschler, J. B., Ladda, R., Sell, S., Martin, J., Ryan, S., Jones, M. C., Moran, R., Shealy, A., Madan-Khetarpal, S., McConnell, J., Surti, U., Delahaye, A., Heron-Longe, B., Pipiras, E., Benzacken, B., Passemard, S., Verloes, A., Isidor, B., Le Caignec, C., Glew, G. M., Opheim, K. E., Descartes, M., Eichler, E. E., Morton, C. C., Gusella, J. F., Schultz, R. A., Ballif, B. C. and Shaffer, L. G. (2012), Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic features. Hum. Mutat., 33: 728–740. doi: 10.1002/humu.22037
- Issue published online: 12 MAR 2012
- Article first published online: 12 MAR 2012
- Accepted manuscript online: 30 JAN 2012 12:00AM EST
- Manuscript Accepted: 11 JAN 2012
- Manuscript Received: 3 OCT 2011
- NIH. Grant Numbers: GM061354 (DGAP; C.C.M), HD065286 (J.F.G.), F32MH087123 (M.E.T.)
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