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Kee C 23
Showing records 1 to 23 | Display all abstracts from Kee C60567 Comparison of visual field progression between temporally tilted disc and nontilted disc, in patients with normal tension glaucoma
Choy YJ
Eye 2015; 29: 1308-1314
60334 Mutations in DDX58, which encodes RIG-I, cause atypical Singleton-Merten syndrome
Jang MA
American Journal of Human Genetics 2015; 96: 266-274
60492 A novel splice site mutation in the PAX6 gene in a Korean family with isolated aniridia
Chang MS
Annals of clinical and laboratory science 2015; 45: 90-93
60103 Comparison of lamina cribrosa thickness in normal tension glaucoma patients with unilateral visual field defect
Kwun Y; Han JC
American Journal of Ophthalmology 2015; 159: 512-8.e1
60334 Mutations in DDX58, which encodes RIG-I, cause atypical Singleton-Merten syndrome
Kim EK
American Journal of Human Genetics 2015; 96: 266-274
60567 Comparison of visual field progression between temporally tilted disc and nontilted disc, in patients with normal tension glaucoma
Kwun Y
Eye 2015; 29: 1308-1314
60492 A novel splice site mutation in the PAX6 gene in a Korean family with isolated aniridia
Han JC
Annals of clinical and laboratory science 2015; 45: 90-93
60567 Comparison of visual field progression between temporally tilted disc and nontilted disc, in patients with normal tension glaucoma
Han JC
Eye 2015; 29: 1308-1314
60492 A novel splice site mutation in the PAX6 gene in a Korean family with isolated aniridia
Lee J
Annals of clinical and laboratory science 2015; 45: 90-93
60334 Mutations in DDX58, which encodes RIG-I, cause atypical Singleton-Merten syndrome
Now H
American Journal of Human Genetics 2015; 96: 266-274
60103 Comparison of lamina cribrosa thickness in normal tension glaucoma patients with unilateral visual field defect
Kee C
American Journal of Ophthalmology 2015; 159: 512-8.e1
60567 Comparison of visual field progression between temporally tilted disc and nontilted disc, in patients with normal tension glaucoma
Kee C
Eye 2015; 29: 1308-1314
60334 Mutations in DDX58, which encodes RIG-I, cause atypical Singleton-Merten syndrome
Nguyen NT
American Journal of Human Genetics 2015; 96: 266-274
60492 A novel splice site mutation in the PAX6 gene in a Korean family with isolated aniridia
Kwun Y
Annals of clinical and laboratory science 2015; 45: 90-93
60334 Mutations in DDX58, which encodes RIG-I, cause atypical Singleton-Merten syndrome
Kim WJ
American Journal of Human Genetics 2015; 96: 266-274
60492 A novel splice site mutation in the PAX6 gene in a Korean family with isolated aniridia
Huh R; Ki CS
Annals of clinical and laboratory science 2015; 45: 90-93
60334 Mutations in DDX58, which encodes RIG-I, cause atypical Singleton-Merten syndrome
Yoo JY
American Journal of Human Genetics 2015; 96: 266-274
60492 A novel splice site mutation in the PAX6 gene in a Korean family with isolated aniridia
Kee C
Annals of clinical and laboratory science 2015; 45: 90-93
60334 Mutations in DDX58, which encodes RIG-I, cause atypical Singleton-Merten syndrome
Lee J
American Journal of Human Genetics 2015; 96: 266-274
60492 A novel splice site mutation in the PAX6 gene in a Korean family with isolated aniridia
Cho SY
Annals of clinical and laboratory science 2015; 45: 90-93
60334 Mutations in DDX58, which encodes RIG-I, cause atypical Singleton-Merten syndrome
Jeong YM
American Journal of Human Genetics 2015; 96: 266-274
60492 A novel splice site mutation in the PAX6 gene in a Korean family with isolated aniridia
Jin DK
Annals of clinical and laboratory science 2015; 45: 90-93
60334 Mutations in DDX58, which encodes RIG-I, cause atypical Singleton-Merten syndrome
Kim CH; Kim OH; Sohn S; Nam SH; Hong Y; Lee YS; Chang SA; Jang SY; Kim JW; Lee MS; Lim SY; Sung KS; Park KT; Kim BJ; Lee JH; Kim DK; Kee C; Ki CS
American Journal of Human Genetics 2015; 96: 266-274
