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American Journal of Ophthalmology|September 4, 1998
Effects of PAX6 mutations on retinal function: an electroretinographic studyF Tremblay, S K Gupta, I De Becker, et al.
American Journal of Ophthalmology|September 4, 1998
Genotype/phenotype correlations in aniridiaS K Gupta, I De Becker, F Tremblay, et al.
American Journal of Ophthalmology|June 13, 1998
Polymerase chain reaction-based risk assessment for Wilms tumor in sporadic aniridiaS K Gupta, I De Becker, D L Guernsey, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|December 22, 1999
A novel PAX6 frameshift mutation in a kindred from Atlantic Canada with familial aniridiaS K Gupta, A Orr, D Bulman, et al.
American Journal of Ophthalmology|April 29, 1998
Lattice corneal dystrophy type 1 in a Canadian kindred is associated with the Arg124 --> Cys mutation in the kerato-epithelin gene. sgupta@ogh.on.caS K Gupta, W G Hodge, K F Damji, et al.
Vision Research|August 1, 1995
The electroretinographic diagnosis of the incomplete form of congenital stationary night blindnessF Tremblay, R G Laroche, I De Becker
Investigative Ophthalmology & Visual Science|August 1, 1996
Visual evoked potentials with crossed asymmetry in incomplete congenital stationary night blindnessF Tremblay, I De Becker, C Cheung, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|December 1, 1994
Duchenne muscular dystrophy: negative scotopic bright-flash electroretinogram but not congenital stationary night blindnessF Tremblay, I De Becker, J M Dooley, et al.
The British Journal of Ophthalmology|September 1, 1994
Correlation between electroretinogram findings and molecular analysis in the Duchenne muscular dystrophy phenotypeI De Becker, D C Riddell, J M Dooley, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|December 1, 1994
Duchenne muscular dystrophy: negative scotopic bright-flash electroretinogram and normal dark adaptationF Tremblay, I De Becker, D C Riddell, et al.
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