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Original article
Whole exome sequencing identifies de novo mutations in GATA6 associated with congenital diaphragmatic hernia

Authors

  1. 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
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Citation

Yu L, Bennett JT, Wynn J, et al
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 
April 27, 2016

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