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Novel deletions of 14q11.2 associated with developmental delay, cognitive impairment and similar minor anomalies in three children
- Correspondence to: Farah 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
Citation
Novel deletions of 14q11.2 associated with developmental delay, cognitive impairment and similar minor anomalies in three children
Publication history
- Received April 4, 2007
- Accepted May 6, 2007
- Revised May 2, 2007
- First published June 1, 2007.
Online issue publication
April 27, 2016
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Copyright 2007 Journal of Medical Genetics