Article info
PDFDevelopmental defects
Original article
Whole exome sequencing identifies de novo mutations in GATA6 associated with congenital diaphragmatic hernia
- Correspondence to Dr Wendy K Chung, Division of Molecular Genetics, Department of Pediatrics, Columbia University Medical Center, 1150 St. Nicholas Avenue, Room 620, New York, NY 10032, USA; wkc15{at}columbia.edu Heather C Mefford, MD, PhD, Division of Genetic Medicine, Department of Pediatrics, University of Washington, 1959 NE Pacific St. Box 356320, Seattle, WA 98115, USA; hmefford@uw.edu
Citation
Whole exome sequencing identifies de novo mutations in GATA6 associated with congenital diaphragmatic hernia
Publication history
- Received August 5, 2013
- Revised October 21, 2013
- Accepted November 7, 2013
- First published January 2, 2014.
Online issue publication
February 14, 2014
Article Versions
- Previous version (2 January 2014).
- You are viewing the most recent version of this article.
Request permissions
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Copyright information
Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions