Show 100 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="Zankl, Andreas" or (type exact bookEditor and editor="Zankl, Andreas") Add to list Conference Paper C3 Identification of a novel COL1A1 mutation associated with Caffey disease Tibbe Dhooge, Delfien Syx (UGent) , Geert Mortier (UGent) , Dagmar Wieczorek, Sheila Unger, Andreas Zankl, Toni Hospach, Sofie Symoens (UGent) and Fransiska Malfait (UGent) (2017) Collagen, Gordon research conference, Abstracts. Add to list Journal Article A2 Whole exome sequencing is an efficient, sensitive and specific method of mutation detection in osteogenesis imperfecta and Marfan syndrome Aideen M Mclnerney-Leo, Mhairi S Marshall, Brooke Gardiner, Paul Coucke (UGent) , Lut Van Laer, Bart L Loeys, Kim M Summers, Sofie Symoens (UGent) , Jennifer A West, Malcolm J West, et al. (2013) BONEKEY REPORTS. 2. 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