How to Cite this Article: Dasouki M, Andrews B, Parimi P, Kamnasaran D. 2013. Recurrent agnathia–otocephaly caused by DNA replication slippage in PRRX1. Am J Med Genet Part A 161A:803–808
Recurrent agnathia–otocephaly caused by DNA replication slippage in PRRX1†
Version of Record online: 26 FEB 2013
Copyright © 2013 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 161, Issue 4, pages 803–808, April 2013
How to Cite
Dasouki, M., Andrews, B., Parimi, P. and Kamnasaran, D. (2013), Recurrent agnathia–otocephaly caused by DNA replication slippage in PRRX1. Am. J. Med. Genet., 161: 803–808. doi: 10.1002/ajmg.a.35879
- Issue online: 19 MAR 2013
- Version of Record online: 26 FEB 2013
- Manuscript Accepted: 2 JAN 2013
- Manuscript Received: 30 MAR 2012
- CHUQ foundation, Fondation des étoiles, Canadian Foundation
- Faculty of Medicine Foundation, Natural Sciences and Engineering Research Council, Laval University
Additional Supporting Information may be found in the online version of this article.
|ajmg_35879_sm_SuppFig1.tif||232K||Fig. 1: Heterozygous frameshift mutations identified in the PRRX1 gene from the genomic DNA of the newborn infant (proband) and father, but absent in the mother and normal individuals (n#100 tested).|
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