Show 5 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="Kerr, Bronwyn" or (type any "bookEditor issueEditor" and editor="Kerr, Bronwyn") Add to list Journal Article A1 open access ACTB loss-of-function mutations result in a pleiotropic developmental disorder Sara Cuvertino, Helen M Stuart, Kate E Chandler, Neil A Roberts, Ruth Armstrong, Laura Bernardini, Sanjeev Bhaskar, Bert Callewaert (UGent) , Jill Clayton-Smith, Cristina Hernando Davalillo, et al. (2017) AMERICAN JOURNAL OF HUMAN GENETICS. 101(6). p.1021-1033 Add to list Journal Article A1 FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly Nicolas Simonis, Isabelle Migeotte, Nelle Lambert, Camille Perazzolo, Deepthi C de Silva, Boyan Dimitrov, Claudine Heinrichs, Sandra Janssens (UGent) , Bronwyn Kerr, Geert Mortier, et al. (2013) JOURNAL OF MEDICAL GENETICS. 50(9). p.585-592 Add to list Journal Article A1 Mutation-based growth charts for SEDC and other COL2A1 related dysplasias Paulien A Terhal, Paula van Dommelen, Martine Le Merrer, Andreas Zankl, Marleen EH Simon, Sarah F Smithson, Carlo Marcelis, Bronwyn Kerr, Esther Kinning, Sahar Mansour, et al. (2012) AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS. 160C(3). p.205-216