Show 250 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="Holder, Graham E*" or (type exact bookEditor and editor="Holder, Graham E*") Add to list Journal Article A1 Disease expression in autosomal recessive retinal dystrophy associated with mutations in the DRAM2 gene Panagiotis I Sergouniotis, Martin McKibbin, Anthony G Robson, Hanno J Bolz, Elfride De Baere (UGent) , Philipp L Müller, Raoul Heller, Mohammed E El-Asrag, Kristof Van Schil (UGent) , Vincent Plagnol, et al. (2015) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. 56(13). p.8083-8090 Add to list Miscellaneous Childhood onset autosomal recessive bestrophinopathy Arundhati Dev Borman, Alice E Davidson, James O'Sullivan, Dorothy A Thompson, Anthony G Robson, Elfride De Baere (UGent) , Graeme CM Black, Andrew R Webster, Graham E Holder, Bart Leroy (UGent) , et al. (2011) ARCHIVES OF OPHTHALMOLOGY. 129(8). p.1088-1093 Add to list Journal Article A1 A detailed phenotypic assessment of individuals affected by MFRP-related oculopathy Rajarshi Mukhopadhyay, Panagiotis I Sergouniotis, Donna S Mackay, Alexander C Day, Genevieve Wright, Sophie Devery, Bart Leroy (UGent) , Anthony G Robson, Graham E Holder, Zheng Li, et al. (2010) MOLECULAR VISION. 16. p.540-548 Add to list Journal Article A1 Pseudoxanthoma elasticum with generalized retinal dysfunction, a common finding? Isabelle Audo, Olivier Vanakker (UGent) , Alaric Smith, Bart Leroy (UGent) , Anthony G Robson, Sharon A Jenkins, Paul Coucke (UGent) , Alan C Bird, Anne De Paepe (UGent) , Graham E Holder, et al. (2007) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. 48(9). p.4250-4256 Add to list Journal Article A1 The phenotype of Leber congenital amaurosis in patients with AIPL1 mutations Sharola Dhamaraj, Bart Leroy (UGent) , Melanie M Sohocki, Robert K Koenekoop, Isabelle Perrault, Khalid Anwar, Shagufta Khaliq, R Summathie Devi, David G Birch, Elaine De Pool, et al. (2004) ARCHIVES OF OPHTHALMOLOGY. 122(7). p.1029-1037