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="Condroyer, Christel" or (type any "bookEditor journalEditor issueEditor" and editor="Cond... Add to list Journal Article A1 open access Loss of function of RIMS2 causes a syndromic congenital cone-rod synaptic disease with neurodevelopmental and pancreatic involvement Sabrina Mechaussier, Basamat Almoallem Mohammed (UGent) , Christina Zeitz, Kristof Van Schil (UGent) , Laila Jeddawi, Jo Van Dorpe (UGent) , Alfredo Dueñas Rey (UGent) , Christel Condroyer, Olivier Pelle, Michel Polak, et al. (2020) AMERICAN JOURNAL OF HUMAN GENETICS. 106(6). p.859-871 Add to list Journal Article A1 Where are the missing gene defects in inherited retinal disorders? : intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders Christina Zeitz, Christelle Michiels, Marion Neuillé, Christoph Friedburg, Christel Condroyer, Fiona Boyard, Aline Antonio, Nassima Bouzidi, Diana Milicevic, Robin Veaux, et al. (2019) HUMAN MUTATION. 40(6). p.765-787 Add to list Journal Article A1 Biallelic mutations in GNB3 cause a unique form of autosomal-recessive congenital stationary night blindness Ajoy Vincent, Isabelle Audo, Erika Tavares, Jason T Maynes, Anupreet Tumber, Thomas Wright, Shuning Li, Christelle Michiels, Christel Condroyer, Heather MacDonald, et al. (2016) AMERICAN JOURNAL OF HUMAN GENETICS. 98(5). p.1011-1019