| Authors: |
Bouasker S; Research Center, University Hospital Centre Sainte-Justine, Montreal H3T 1C5, Québec, Canada., Patel N; Department of Translational Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Greenlees R; Eye Genetics Research Unit, Children's Medical Research Institute, University of Sydney; The Children's Hospital at Westmead, Sydney Children's Hospitals Network; and Save Sight Institute, Sydney, New South Wales, Australia., Wellesley D; Wessex Clinical Genetic Service, University Hospital Southampton, Southampton, UK., Fares Taie L; Laboratory Genetics in Ophthalmology, INSERM UMR1163, Imagine Institute for Genetic Diseases, Université Paris Descartes-Sorbonne, Paris, Île-de-France, France., Almontashiri NA; Center for Genetics and Inherited Diseases (CGID), Taibah University, Madinah, Al Madinah, Saudi Arabia.; Research Department, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia., Baptista J; Peninsula Medical School, Faculty of Health, University of Plymouth, Plymouth, UK.; Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter, UK., Alghamdi MA; Medical Genetic Division, Pediatric Department, College of Medicine, King Saud University, Riyadh, Saudi Arabia., Boissel S; Research Center, University Hospital Centre Sainte-Justine, Montreal H3T 1C5, Québec, Canada., Martinovic J; Unit of Fetal Pathology, APHP Hopital Antoine-Beclere, Clamart, Île-de-France, France., Prokudin I; Eye Genetics Research Unit, Children's Medical Research Institute, University of Sydney; The Children's Hospital at Westmead, Sydney Children's Hospitals Network; and Save Sight Institute, Sydney, New South Wales, Australia., Holden S; Department of Cellular Pathology, University Hospital Southampton, Southampton, UK., Mudhar HS; National Specialist Ophthalmic Pathology Service (NSOPS), Dept of Histopathology, Royal Hallamshire Hospital, Sheffield, UK., Riley LG; Rare Diseases Functional Genomics Laboratory, The Children's Hospital at Westmead, Sydney Children's Hospitals Network, Children's Medical Research Institute, University of Sydney, Sydney, New South Wales, Australia.; Specialty of Paediatrics and Child Health, Faculty of Medicine and Health, University of Sydney, Sidney, New South Wales, Australia., Nassif C; Research Center, University Hospital Centre Sainte-Justine, Montreal H3T 1C5, Québec, Canada., Attie-Bitach T; Laboratory of Embryology and Genetics of Congenital Malformations, INSERM UMR 1163, Imagine Institute for Genetic Diseases, Paris, Île-de-France, France., Miguet M; Research Center, University Hospital Centre Sainte-Justine, Montreal H3T 1C5, Québec, Canada., Delous M; Equipe GENDEV, Centre de Recherche en Neurosciences de Lyon, Inserm U1028, CNRS UMR5292, Université Lyon 1, Université St Etienne, Lyon, Auvergne-Rhône-Alpes, France., Ernest S; Laboratory of Embryology and Genetics of Congenital Malformations, INSERM UMR 1163, Imagine Institute for Genetic Diseases, Paris, Île-de-France, France., Plaisancié J; Department of Medical Genetics, Purpan University Hospital, Toulouse, Midi-Pyrénées, France.; Centre de Référence des Affections Rares en Génétique Ophtalmologique CARGO, Site Constitutif, Purpan University Hospital, Toulouse, Midi-Pyrénées, France.; INSERM U1214, ToNIC, Université Toulouse III, Toulouse, France., Calvas P; Department of Medical Genetics, Purpan University Hospital, Toulouse, Midi-Pyrénées, France.; Centre de Référence des Affections Rares en Génétique Ophtalmologique CARGO, Site Constitutif, Purpan University Hospital, Toulouse, Midi-Pyrénées, France., Rozet JM; Laboratory Genetics in Ophthalmology, INSERM UMR1163, Imagine Institute for Genetic Diseases, Université Paris Descartes-Sorbonne, Paris, Île-de-France, France., Khan AO; Eye Institute, Cleveland Clinic Abu Dhabi, Abu Dhabi, Abu Dhabi, UAE., Hamdan FF; Research Center, University Hospital Centre Sainte-Justine, Montreal H3T 1C5, Québec, Canada., Jamieson RV; Eye Genetics Research Unit, Children's Medical Research Institute, University of Sydney; The Children's Hospital at Westmead, Sydney Children's Hospitals Network; and Save Sight Institute, Sydney, New South Wales, Australia.; Specialty of Genomic Medicine, Faculty of Medicine and Health and Child and Adolescent Health, University of Sydney, Sydney, New South Wales, Australia., Alkuraya FS; Department of Translational Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia chassaing.n@chu-toulouse.fr jacques.michaud.med@ssss.gouv.qc.ca FAlKuraya@kfshrc.edu.sa.; Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia., Michaud JL; Departments of Pediatrics and Neurosciences, Université de Montréal, Montreal H3T 1J4, Québec, Canada chassaing.n@chu-toulouse.fr jacques.michaud.med@ssss.gouv.qc.ca FAlKuraya@kfshrc.edu.sa.; Departments of Pediatrics and Neurosciences, Université de Montréal, Montreal, Québec, Canada., Chassaing N; Department of Medical Genetics, Purpan University Hospital, Toulouse, Midi-Pyrénées, France chassaing.n@chu-toulouse.fr jacques.michaud.med@ssss.gouv.qc.ca FAlKuraya@kfshrc.edu.sa.; Centre de Référence des Affections Rares en Génétique Ophtalmologique CARGO, Site Constitutif, Purpan University Hospital, Toulouse, Midi-Pyrénées, France. |
