How to Cite this Article: Castronovo C, Rusconi D, Crippa M, Giardino D, Gervasini C, Milani D, Cereda A, Larizza L, Selicorni A, Finelli P. 2013. A novel mosaic NSD1 intragenic deletion in a patient with an atypical phenotype. Am J Med Genet Part A 161A: 611–618.
Article first published online: 22 JAN 2013
Copyright © 2013 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 161, Issue 3, pages 611–618, March 2013
How to Cite
Castronovo, C., Rusconi, D., Crippa, M., Giardino, D., Gervasini, C., Milani, D., Cereda, A., Larizza, L., Selicorni, A. and Finelli, P. (2013), A novel mosaic NSD1 intragenic deletion in a patient with an atypical phenotype. Am. J. Med. Genet., 161: 611–618. doi: 10.1002/ajmg.a.35814
All authors declare that they have no conflicts of interest.
- Issue published online: 21 FEB 2013
- Article first published online: 22 JAN 2013
- Manuscript Accepted: 14 NOV 2012
- Manuscript Received: 7 SEP 2011
- Ministry of Health. Grant Number: 08C101_2011
Additional supporting information may be found in the online version of this article.
|ajmg_35814_sm_SupplFigS1.tif||1508K||eFig. 1S: Physical reciprocal position of the probes centromere-RP11-1021M23, (blue)-CTD-2552L10, (red)-RP11-281O15, and (green)-telomere, showing an inverted reference sequence order of the probes CTD-2552L10 (red) and RP11-281O15 (green), in one allele in a small percentage of cells (arrows).|
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