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Suri F 12
Showing records 1 to 12 | Display all abstracts from Suri F95979 Prenatal diagnosis of primary congenital glaucoma and histopathological features in a fetal globe with mutations
Rezaei Kanavi M
European Journal of Ophthalmology 2021; 0: 11206721211051235
96362 Carrier Status for p.Gly61Glu and p.Arg368His Mutations Causing Primary Congenital Glaucoma in Iran
Heshmati A
Journal of ophthalmic & vision research 2021; 16: 574-581
95979 Prenatal diagnosis of primary congenital glaucoma and histopathological features in a fetal globe with mutations
Yazdani S
European Journal of Ophthalmology 2021; 0: 11206721211051235
96362 Carrier Status for p.Gly61Glu and p.Arg368His Mutations Causing Primary Congenital Glaucoma in Iran
Taghizadeh P
Journal of ophthalmic & vision research 2021; 16: 574-581
95979 Prenatal diagnosis of primary congenital glaucoma and histopathological features in a fetal globe with mutations
Elahi E
European Journal of Ophthalmology 2021; 0: 11206721211051235
96362 Carrier Status for p.Gly61Glu and p.Arg368His Mutations Causing Primary Congenital Glaucoma in Iran
Ahmadieh H; Yaseri M
Journal of ophthalmic & vision research 2021; 16: 574-581
95979 Prenatal diagnosis of primary congenital glaucoma and histopathological features in a fetal globe with mutations
Mirrahimi M
European Journal of Ophthalmology 2021; 0: 11206721211051235
96362 Carrier Status for p.Gly61Glu and p.Arg368His Mutations Causing Primary Congenital Glaucoma in Iran
Suri F
Journal of ophthalmic & vision research 2021; 16: 574-581
95979 Prenatal diagnosis of primary congenital glaucoma and histopathological features in a fetal globe with mutations
Hajizadeh M; Khodaverdi S
European Journal of Ophthalmology 2021; 0: 11206721211051235
96362 Carrier Status for p.Gly61Glu and p.Arg368His Mutations Causing Primary Congenital Glaucoma in Iran
Alizadeh M; Dadashzadeh M
Journal of ophthalmic & vision research 2021; 16: 574-581
95979 Prenatal diagnosis of primary congenital glaucoma and histopathological features in a fetal globe with mutations
Suri F
European Journal of Ophthalmology 2021; 0: 11206721211051235
96362 Carrier Status for p.Gly61Glu and p.Arg368His Mutations Causing Primary Congenital Glaucoma in Iran
Khatami H; Navi MM; Zamanparvar P; Behboudi H; Elahi E
Journal of ophthalmic & vision research 2021; 16: 574-581
