Conflict of interest: none.
Contiguous gene deletion of TBX5 and TBX3 leads to a varible phenotype with combined features of holt-oram and ulnar-mammary syndromes
Article first published online: 24 MAY 2013
Copyright © 2013 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 161, Issue 7, pages 1797–1802, July 2013
How to Cite
2013. Contiguous gene deletion of TBX5 and TBX3 leads to a varible phenotype with combined features of Holt-Oram and ulnar-mammary syndromes. Am J Med Genet Part A 161A:1797–1802., , , , , , , , , , , .
- Issue published online: 19 JUN 2013
- Article first published online: 24 MAY 2013
- Manuscript Accepted: 28 APR 2013
- Manuscript Received: 21 AUG 2012
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