The authors have no conflicts to disclose.
Evaluating rare coding variants as contributing causes to non-syndromic cleft lip and palate
Article first published 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 published online: 17 OCT 2013
- Article first published 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.|
Please note: Wiley Blackwell is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.