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Soucy M 7
Showing records 1 to 7 | Display all abstracts from Soucy M108080 Phenotypic Variability of Retinal Disease Among a Cohort of Patients With Variants in the CLN Genes
Kolesnikova M
Investigative Ophthalmology and Visual Science 2023; 64: 23
107457 Phenotypic variability in PRPH2 as demonstrated by a family with incomplete penetrance of autosomal dominant cone-rod dystrophy
Soucy M
Documenta Ophthalmologica 2023; 146: 267-272
108080 Phenotypic Variability of Retinal Disease Among a Cohort of Patients With Variants in the CLN Genes
Kolesnikova M; Lima de Carvalho JR
Investigative Ophthalmology and Visual Science 2023; 64: 23
107457 Phenotypic variability in PRPH2 as demonstrated by a family with incomplete penetrance of autosomal dominant cone-rod dystrophy
Kolesnikova M; Kolesnikova M; Kim AH
Documenta Ophthalmologica 2023; 146: 267-272
108080 Phenotypic Variability of Retinal Disease Among a Cohort of Patients With Variants in the CLN Genes
Oh JK
Investigative Ophthalmology and Visual Science 2023; 64: 23
107457 Phenotypic variability in PRPH2 as demonstrated by a family with incomplete penetrance of autosomal dominant cone-rod dystrophy
Kim AH; Tsang SH
Documenta Ophthalmologica 2023; 146: 267-272
108080 Phenotypic Variability of Retinal Disease Among a Cohort of Patients With Variants in the CLN Genes
Soucy M; Demirkol A; Kim AH; Kim AH; Tsang SH; Breazzano MP
Investigative Ophthalmology and Visual Science 2023; 64: 23
