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PDFPhenotypes
Original article
WAC loss-of-function mutations cause a recognisable syndrome characterised by dysmorphic features, developmental delay and hypotonia and recapitulate 10p11.23 microdeletion syndrome
- Correspondence to Dr Marwan Shinawi, Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine, One Children's Place, Northwest Tower, 9132, Campus Box 8116, St Louis, MO 63110, USA; Shinawi_M{at}kids.wustl.edu
Citation
WAC loss-of-function mutations cause a recognisable syndrome characterised by dysmorphic features, developmental delay and hypotonia and recapitulate 10p11.23 microdeletion syndrome
Publication history
- Received February 16, 2015
- Revised June 17, 2015
- Accepted July 14, 2015
- First published August 11, 2015.
Online issue publication
October 22, 2015
Article Versions
- Previous version (11 August 2015).
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