All authors have no conflicts of interest.
Identification of single gene deletions at 15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotype
Version of Record online: 7 AUG 2012
© 2012 John Wiley & Sons A/S. Published by Blackwell Publishing Ltd
Volume 83, Issue 4, pages 345–351, April 2013
How to Cite
Identification of single gene deletions at 15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotype, , , , .
- Issue online: 12 MAR 2013
- Version of Record online: 7 AUG 2012
- Accepted manuscript online: 9 JUL 2012 08:45AM EST
- Manuscript Revised: 29 JUN 2012
- Manuscript Accepted: 29 JUN 2012
- Manuscript Received: 5 APR 2012
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