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 exact 05FC2AB6-F0EE-11E1-A9DE-61C894A0A6B4 cql: author exact F621FF76-F0ED-11E1-A9DE-61C894A0A6B4 Add to list Journal Article A1 open access EMILIN1 deficiency causes arterial tortuosity with osteopenia and connects impaired elastogenesis with defective collagen fibrillogenesis Christin S. Adamo, Aude Beyens (UGent) , Alvise Schiavinato, Douglas R. Keene, Sara F. Tufa, Matthias Morgelin, Jurgen Brinckmann, Takako Sasaki, Anja Niehoff, Maren Dreiner, et al. (2022) AMERICAN JOURNAL OF HUMAN GENETICS. 109(12). p.2230-2252 Add to list Journal Article A1 open access Defining the clinical, molecular and ultrastructural characteristics in occipital horn syndrome : two new cases and review of the literature Aude Beyens (UGent) , Kyaran Van Meensel, Lore Pottie (UGent) , Riet De Rycke (UGent) , Michiel De Bruyne (UGent) , Femke Baeke (UGent) , Piet Hoebeke (UGent) , Frank Plasschaert (UGent) , Bart Loeys, Sofie De Schepper (UGent) , et al. (2019) GENES. 10(7).