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="Black, GCM" or (type any "bookEditor issueEditor" and editor="Black, GCM") Add to list Journal Article A1 Biallelic mutation of BEST1 causes a distinct retinopathy in humans R Burgess, ID Millar, Bart Leroy (UGent) , JE Urquhart, IM Fearon, Elfride De Baere (UGent) , PD Brown, AG Robson, GA Wright, PHILIPPE ADRIAAN KESTELYN (UGent) , et al. (2008) AMERICAN JOURNAL OF HUMAN GENETICS. 82(1). p.19-31 Add to list Journal Article A1 Intrafamilial phenotypic variability in families with RDS mutations: exclusion of ROM1 as a genetic modifier for those with retinitis pigmentosa Bart Leroy (UGent) , A Kailasanathan, Jean Delaey (UGent) , GCM Black and FDC Manson (2007) BRITISH JOURNAL OF OPHTHALMOLOGY. 91(1). p.89-93 Add to list Conference Paper C3 Mutations in VMD2 cause autosomal dominant vitreoretinochoroidopathy (ADVIRC) Bart Leroy (UGent) , J YARDLEY, N HART-HOLDEN, Bart Lafaut, B PUECH, MA REDDY, Jean Delaey (UGent) , Philippe Kestelyn (UGent) , AT MOORE and GCM BLACK (2005) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. 46.