1. Dominant retinitis pigmentosa phenotype associated with a new mutation in the splicing factor PRPF31. Issue 10 (25th September 2007) Authors: Ghazawy, S; Springell, K; Gauba, V; McKibbin, M A; Inglehearn, C F Journal: British journal of ophthalmology Issue: Volume 91:Issue 10(2007) Page Start: 1411 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Further considerations of retinopathy with renal failure. Issue 5 (1st May 2003) Authors: Mohamed, M D; McKibbin, M A Journal: British journal of ophthalmology Issue: Volume 87:Issue 5(2003) Page Start: 659 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Progession of phenotype in Leber's congenital amaurosis with a mutation at the LCA5 locus. Issue 4 (1st April 2003) Authors: Mohamed, M D; Topping, N C; Jafri, H; Raashed, Y; McKibbin, M A; Inglehearn, C F Journal: British journal of ophthalmology Issue: Volume 87:Issue 4(2003) Page Start: 473 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗