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Hejtmancik JF 15
Showing records 1 to 15 | Display all abstracts from Hejtmancik JF105821 Truncation mutations in MYRF underlie primary angle closure glaucoma
Ouyang J
Human Genetics 2023; 142: 103-123
106059 Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma
Rauf B
Scientific reports 2022; 12: 17218
105821 Truncation mutations in MYRF underlie primary angle closure glaucoma
Sun W
Human Genetics 2023; 142: 103-123
106059 Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma
Khan SY; Jiao X
Scientific reports 2022; 12: 17218
105821 Truncation mutations in MYRF underlie primary angle closure glaucoma
Shen H; Liu X
Human Genetics 2023; 142: 103-123
106059 Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma
Irum B; Ashfaq R
Scientific reports 2022; 12: 17218
105821 Truncation mutations in MYRF underlie primary angle closure glaucoma
Wu Y; Jiang H
Human Genetics 2023; 142: 103-123
106059 Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma
Zehra M
Scientific reports 2022; 12: 17218
105821 Truncation mutations in MYRF underlie primary angle closure glaucoma
Li X
Human Genetics 2023; 142: 103-123
106059 Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma
Khan AA; Naeem MA
Scientific reports 2022; 12: 17218
105821 Truncation mutations in MYRF underlie primary angle closure glaucoma
Wang Y; Jiang Y
Human Genetics 2023; 142: 103-123
106059 Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma
Shahzad M; Riazuddin S
Scientific reports 2022; 12: 17218
105821 Truncation mutations in MYRF underlie primary angle closure glaucoma
Li S; Xiao X
Human Genetics 2023; 142: 103-123
106059 Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma
Hejtmancik JF; Riazuddin SA
Scientific reports 2022; 12: 17218
105821 Truncation mutations in MYRF underlie primary angle closure glaucoma
Hejtmancik JF; Tan Z; Zhang Q
Human Genetics 2023; 142: 103-123
