The role of putative Tbx1 traget genes in the pathogenesis of the 22q11 deletion syndrome phenotype
The 22q11 deletion syndrome (22q11DS/DiGeorge Syndrome [DGS]) is a congenital disorder with complex aetiology including cardiovascular, thymic/parathyroid, craniofacial and neuro-behavioural phenotypes. These arise via abnormal development of embryonic structures including the pharyngeal arch/artery...
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University College London (University of London)
2013
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| Online Access: | http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.626150 |