Investigating a Tbx1 and Pax9 genetic interaction during cardiovascular development
Congenital cardiovascular malformations (CCVM) are the most common type of birth defect in humans and can be life threatening for the newborn. 22q11 deletion syndrome (22q11DS) is one of the most common CCVM in humans, with patients presenting a wide variety of abnormalities including craniofacial d...
| Main Author: | |
|---|---|
| Published: |
University of Newcastle upon Tyne
2015
|
| Subjects: | |
| Online Access: | http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.680309 |