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="Kahrizi, K*" or (type exact bookEditor and editor="Kahrizi, K*") Add to list Journal Article A1 Redefining the MED13L syndrome Abidemi Adegbola, Luciana Musante, Bert Callewaert (UGent) , Patricia Maciel, Hao Hu, Bertrand Isidor, Sylvie Picker-Minh, Cedric Le Caignec, Barbara Delle Chiaie, Olivier Vanakker (UGent) , et al. (2015) EUROPEAN JOURNAL OF HUMAN GENETICS. 23(10). p.1308-1317 Add to list Journal Article A1 Expanded mutational spectrum in Cohen syndrome, tissue expression, and transcript variants of COH1 Wenke Seifert, Muriel Holder-Espinasse, Jirko Kühnisch, Kimia Kahrizi, Andreas Tzschach, Masoud Garshasbi, Hossein Najambadi, Andreas Walter Kuss, Wolfram Kress, Genevieve Laureys (UGent) , et al. (2009) HUMAN MUTATION. 30(2). p.E404-E420 Add to list Journal Article A1 A novel DFNA5 mutation does not cause hearing loss in an Iranian family Lut Van Laer (UGent) , NC Meyer, M Malekpour, Y Riazalhosseini, M Moghannibashi, K Kahrizi, A Vandevelde, F Alasti, H Najmabadi, G Van Camp, et al. (2007) JOURNAL OF HUMAN GENETICS. 52(6). p.549-552