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Ki CS 13
Showing records 1 to 13 | Display all abstracts from Ki CS60334 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; Han JC
Annals of clinical and laboratory science 2015; 45: 90-93
60334 Mutations in DDX58, which encodes RIG-I, cause atypical Singleton-Merten syndrome
Kim EK
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
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; 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; Huh R
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; 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
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
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
Kee C; 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; Kim CH
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 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
