Further considerations of retinopathy with renal failure

od Mohamed, M D, McKibbin, M A
Wydane 2003

Dominant retinitis pigmentosa phenotype associated with a new mutation in the splicing factor PRPF31

od Ghazawy, S, Springell, K, Gauba, V, McKibbin, M A, Inglehearn, C F
Wydane 2007

Progession of phenotype in Leber’s congenital amaurosis with a mutation at the LCA5 locus

od Mohamed, M D, Topping, N C, Jafri, H, Raashed, Y, McKibbin, M A, Inglehearn, C F
Wydane 2003