Show 10 5 10 15 20 50 100 250 Sort by year (new to old) Actions Download search results Subscribe to news feed Your filters: cql: author="Menon, Swapna" or (type exact bookEditor and editor="Menon, Swapna") Add to list Journal Article A1 open access Characterization of a distinct lethal arteriopathy syndrome in twenty-two infants associated with an identical, novel mutation in FBLN4 gene, confirms fibulin-4 as a critical determinant of human vascular elastogenesis Mahesh Kappanayil, Sheela Nampoothiri, Rajesh Kannan, Marjolijn Renard (UGent) , Paul Coucke (UGent) , Fransiska Malfait (UGent) , Swapna Menon, Hiran K Ravindran, Renu Kurup, Muhammad Faiyaz-Ul-Haque, et al. (2012) ORPHANET JOURNAL OF RARE DISEASES. 7.