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Hartill, Verity Laura
Congenital Heart Disease (CHD) is the most common congenital defect, but the genetic aetiology of a large proportion of CHD is unexplained. This project aimed to delineate novel genetic causes of CHD using Whole Exome Sequencing (WES) in a family-bas
Externí odkaz:
https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.727216
