The authors have no conflicts to disclose.
Evaluating rare coding variants as contributing causes to non-syndromic cleft lip and palate
Version of Record online: 10 OCT 2012
© 2012 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
Special Issue: Variant
Volume 84, Issue 5, pages 496–500, November 2013
How to Cite
Evaluating rare coding variants as contributing causes to non-syndromic cleft lip and palate., .
- Issue online: 17 OCT 2013
- Version of Record online: 10 OCT 2012
- Accepted manuscript online: 14 SEP 2012 08:52AM EST
- Manuscript Revised: 11 SEP 2012
- Manuscript Accepted: 11 SEP 2012
- Manuscript Received: 9 JUL 2012
- NIH. Grant Numbers: R37-DE008559, U01-DE020057
|cge12018-sup-0001-TableS1.doc||Word document||225K||Table S1. Genes with rare missense, nonsense, or splice variants reported in NSCL/P.|
|cge12018-sup-0002-TableS2.doc||Word document||183K||Table S2. Variant positions for genes with updated RefSeq transcripts.|
|cge12018-sup-0003-TableS3.doc||Word document||223K||Table S3. Variants previously reported in NSCL/P cases and population or CEPH controls.|
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