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="Traboulsi, Elias" or (type exact bookEditor and editor="Traboulsi, Elias") Add to list Journal Article A1 open access Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia Maria Solaki, Britta Baumann, Peggy Reuter, Sten Andreasson, Isabelle Audo, Carmen Ayuso, Ghassan Balousha, Francesco Benedicenti, David Birch, Pierre Bitoun, et al. (2022) HUMAN MUTATION. 43(7). p.832-858 Add to list Journal Article A1 Homozygous stop mutation in AHR causes autosomal recessive foveal hypoplasia and infantile nystagmus Anja K. Mayer, Muhammad Mahajnah, Mervyn G. Thomas, Yuval Cohen, Adib Habib, Martin Schulze, Gail D. E. Maconachie, Basamat Almoallem Mohammed (UGent) , Elfride De Baere (UGent) , Birgit Lorenz, et al. (2019) BRAIN. 142(6). p.1528-1534 Add to list Journal Article A1 Mutations of VMD2 splicing regulators cause nanophthalmos and autosomal dominant vitreoretinochoroidopathy (ADVIRC) Jill Yardley, Bart Leroy (UGent) , Niki Hart-Holden, Bart Lafaut, Bart Loeys (UGent) , Ludwine Messiaen, Rahat Perveen, M Ashwin Reddy, Shomi S Bhattacharya, Elias Traboulsi, et al. (2004) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. 45(10). p.3683-3689