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Hejtmancik JF 19

Showing records 1 to 19 | Display all abstracts from Hejtmancik JF

105821 Truncation mutations in MYRF underlie primary angle closure glaucoma
Ouyang J
Human Genetics 2023; 142: 103-123

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106059 Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma
Rauf B; Khan SY
Scientific reports 2022; 12: 17218

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105821 Truncation mutations in MYRF underlie primary angle closure glaucoma
Sun W; Shen H
Human Genetics 2023; 142: 103-123

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106059 Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma
Jiao X; Irum B
Scientific reports 2022; 12: 17218

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105821 Truncation mutations in MYRF underlie primary angle closure glaucoma
Liu X
Human Genetics 2023; 142: 103-123

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106059 Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma
Ashfaq R
Scientific reports 2022; 12: 17218

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105821 Truncation mutations in MYRF underlie primary angle closure glaucoma
Wu Y
Human Genetics 2023; 142: 103-123

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106059 Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma
Zehra M
Scientific reports 2022; 12: 17218

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105821 Truncation mutations in MYRF underlie primary angle closure glaucoma
Jiang H; Li X
Human Genetics 2023; 142: 103-123

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106059 Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma
Khan AA
Scientific reports 2022; 12: 17218

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105821 Truncation mutations in MYRF underlie primary angle closure glaucoma
Wang Y
Human Genetics 2023; 142: 103-123

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106059 Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma
Naeem MA
Scientific reports 2022; 12: 17218

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105821 Truncation mutations in MYRF underlie primary angle closure glaucoma
Jiang Y
Human Genetics 2023; 142: 103-123

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106059 Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma
Shahzad M; Riazuddin S
Scientific reports 2022; 12: 17218

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105821 Truncation mutations in MYRF underlie primary angle closure glaucoma
Li S; Xiao X
Human Genetics 2023; 142: 103-123

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106059 Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma
Hejtmancik JF
Scientific reports 2022; 12: 17218

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105821 Truncation mutations in MYRF underlie primary angle closure glaucoma
Hejtmancik JF
Human Genetics 2023; 142: 103-123

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106059 Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma
Riazuddin SA
Scientific reports 2022; 12: 17218

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105821 Truncation mutations in MYRF underlie primary angle closure glaucoma
Tan Z; Zhang Q
Human Genetics 2023; 142: 103-123

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