You are here

Article info

Article menu
Download PDFPDF
Original article
Velopharyngeal insufficiency: high detection rate of genetic abnormalities if associated with additional features

Authors

  1. Correspondence to Dr Charlotte W Ockeloen, Department of Human Genetics, Radboud University Nijmegen Medical Centre, P.O. Box 9101, Nijmegen 6500 HB, The Netherlands; charlotte.ockeloen{at}radboudumc.nl
View Full Text

Citation

Ockeloen CW, Simpson J, Urquhart J, et al
Velopharyngeal insufficiency: high detection rate of genetic abnormalities if associated with additional features
Archives of Disease in Childhood 2014;99:52-57.

Publication history

  • Received May 23, 2013
  • Revised September 24, 2013
  • Accepted September 26, 2013
  • First published October 21, 2013.
Online issue publication 
March 22, 2016

Article Versions

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