14:45 | A common NYX mutation in Flemish patients with X-linked CSNB | LEROY BP, BUDDE BS, WITTMER M, DE BAERE E, BERGER W, ZEITZ C | ||
14:55 | Genotype-phenotype correlation of Stickler syndrome caused by mutations in the COL2A1 gene | HOORNAERT KP, DEWINTER C, VEREECKE I, VAN AKEN EH, LEROY BP, COUCKE PJ, MORTIER GR | ||
15:05 | Maternally inherited diabetes and deafness associated with ptosis | ROBBERECHT KR, DECOCK CE, SENECA S, DE BLEECKER J, LEROY BP | ||
15:15 | Ocular Findings of Primary Oxalosis in Three Children | DELBEKE P, RAES A, LEROY BP |