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Ophthalmic Genetics 31
Showing records 1 to 25 | Display all abstracts in Ophthalmic Genetics117485 A novel gene variant in a Turkish family with juvenile-onset open-angle glaucoma
Bozkurt B
Ophthalmic Genetics 2024; 0: 1-6
117938 Association of , polymorphisms with POAG and NTG
Samoylov AN
Ophthalmic Genetics 2024; 45: 23-27
118431 GAPO syndrome: a novel variant in ANTXR1 gene
Damagatla M
Ophthalmic Genetics 2024; 0: 1-6
117252 Heterozygous Pyrin (MEFV) E148Q allele carriers indicate a reduced glaucoma risk for Turkish population: a prospective clinical analysis
Muhsinoglu O
Ophthalmic Genetics 2024; 0: 1-5
117605 Primary congenital glaucoma in two siblings with different compound heterozygous CYP1B1 genotypes
Ruiz Guijosa A
Ophthalmic Genetics 2024; 0: 1-4
117375 Consolidating data on the association of IL-6 and IL-10 polymorphisms with the development of glaucoma: a meta-analysis
Golshan-Tafti A
Ophthalmic Genetics 2024; 0: 1-11
117938 Association of , polymorphisms with POAG and NTG
Tumanova P
Ophthalmic Genetics 2024; 45: 23-27
117375 Consolidating data on the association of IL-6 and IL-10 polymorphisms with the development of glaucoma: a meta-analysis
Bahrami M
Ophthalmic Genetics 2024; 0: 1-11
117252 Heterozygous Pyrin (MEFV) E148Q allele carriers indicate a reduced glaucoma risk for Turkish population: a prospective clinical analysis
Akalin I
Ophthalmic Genetics 2024; 0: 1-5
118431 GAPO syndrome: a novel variant in ANTXR1 gene
Verma A
Ophthalmic Genetics 2024; 0: 1-6
117485 A novel gene variant in a Turkish family with juvenile-onset open-angle glaucoma
Bağcı O
Ophthalmic Genetics 2024; 0: 1-6
117605 Primary congenital glaucoma in two siblings with different compound heterozygous CYP1B1 genotypes
Fernández LM
Ophthalmic Genetics 2024; 0: 1-4
117938 Association of , polymorphisms with POAG and NTG
Pankratova SA
Ophthalmic Genetics 2024; 45: 23-27
117375 Consolidating data on the association of IL-6 and IL-10 polymorphisms with the development of glaucoma: a meta-analysis
Mohsenzadeh-Yazdi R
Ophthalmic Genetics 2024; 0: 1-11
118431 GAPO syndrome: a novel variant in ANTXR1 gene
Pochaboina V
Ophthalmic Genetics 2024; 0: 1-6
117252 Heterozygous Pyrin (MEFV) E148Q allele carriers indicate a reduced glaucoma risk for Turkish population: a prospective clinical analysis
Karadag R
Ophthalmic Genetics 2024; 0: 1-5
117485 A novel gene variant in a Turkish family with juvenile-onset open-angle glaucoma
Üzüm S
Ophthalmic Genetics 2024; 0: 1-6
117605 Primary congenital glaucoma in two siblings with different compound heterozygous CYP1B1 genotypes
Martínez de la Casa JM
Ophthalmic Genetics 2024; 0: 1-4
117375 Consolidating data on the association of IL-6 and IL-10 polymorphisms with the development of glaucoma: a meta-analysis
Dastgheib SA
Ophthalmic Genetics 2024; 0: 1-11
117485 A novel gene variant in a Turkish family with juvenile-onset open-angle glaucoma
Çora T
Ophthalmic Genetics 2024; 0: 1-6
117938 Association of , polymorphisms with POAG and NTG
Ashryatova LS
Ophthalmic Genetics 2024; 45: 23-27
118431 GAPO syndrome: a novel variant in ANTXR1 gene
Bhate M
Ophthalmic Genetics 2024; 0: 1-6
117252 Heterozygous Pyrin (MEFV) E148Q allele carriers indicate a reduced glaucoma risk for Turkish population: a prospective clinical analysis
Yilmaz S
Ophthalmic Genetics 2024; 0: 1-5
117605 Primary congenital glaucoma in two siblings with different compound heterozygous CYP1B1 genotypes
Escribano J
Ophthalmic Genetics 2024; 0: 1-4
117252 Heterozygous Pyrin (MEFV) E148Q allele carriers indicate a reduced glaucoma risk for Turkish population: a prospective clinical analysis
Bayramlar H
Ophthalmic Genetics 2024; 0: 1-5
