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Hejtmancik JF 18

Showing records 1 to 18 | Display all abstracts from Hejtmancik JF

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

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105821 Truncation mutations in MYRF underlie primary angle closure glaucoma
Ouyang J; Sun W
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 SY; Jiao X
Scientific reports 2022; 12: 17218

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105821 Truncation mutations in MYRF underlie primary angle closure glaucoma
Shen H; 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
Irum B
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
Ashfaq R
Scientific reports 2022; 12: 17218

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105821 Truncation mutations in MYRF underlie primary angle closure glaucoma
Jiang 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
Zehra M; Khan AA
Scientific reports 2022; 12: 17218

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105821 Truncation mutations in MYRF underlie primary angle closure glaucoma
Li X; 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; Shahzad M
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
Riazuddin S
Scientific reports 2022; 12: 17218

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105821 Truncation mutations in MYRF underlie primary angle closure glaucoma
Li S
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
Xiao X; 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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