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A patient with vertebral, cognitive and behavioural abnormalities and a de novo deletion of NRXN1α

Authors

  1. Ms F Zahir, Medical Genetics Research Unit, University of British Columbia, Box 153, Children’s and Women’s Hospital, 4500 Oak Street, Vancouver, BC, Canada, V6H 3N1; farahz{at}interchange.ubc.ca
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Citation

Zahir FR, Baross A, Delaney AD, et al
A patient with vertebral, cognitive and behavioural abnormalities and a de novo deletion of NRXN1α
Journal of Medical Genetics 2008;45:239-243.

Publication history

  • Received September 8, 2007
  • Revised November 14, 2007
  • Accepted November 16, 2007
  • First published December 5, 2007.
Online issue publication 
April 27, 2016

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2008 BMJ Publishing Group