Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: CRYGD[original query] |
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Mutation analysis of the genes associated with anterior segment dysgenesis, microcornea and microphthalmia in 257 patients with glaucoma. International journal of molecular medicine 2015 Oct 36 (4): 1111-7. Huang Xiaobo, Xiao Xueshan, Jia Xiaoyun, Li Shiqiang, Li Miaoling, Guo Xiangming, Liu Xing, Zhang Qingjio |
Clinical and genetic characteristics of Chinese patients with familial or sporadic pediatric cataract. Orphanet journal of rare diseases 2018 6 13 (1): 94. Li Jingyan, Leng Yunji, Han Shirui, Yan Lulu, Lu Chaoxia, Luo Yang, Zhang Xue, Cao Lih |
Mutation screening of crystallin genes in Chinese families with congenital cataracts. Molecular vision 2019 9 25 427-437. Zhuang Jianfu, Cao Zongfu, Zhu Yihua, Liu Lijuan, Tong Yi, Chen Xiaole, Wang Yaduan, Lu Cailing, Ma Xu, Yang Juh |
Crystalline gene mutations in Turkish children with congenital cataracts. International ophthalmology 2021 4 41 (8): 2847-2852. Karahan Mine, Demirta? At?l?m Arma?an, Erdem Seyfettin, Ava Sedat, Teke? Selahattin, Keklikçi U? |
Novel Likely Pathogenic Variants Identified by Panel-Based Exome Sequencing in Congenital Cataract Patients. Journal of ophthalmology 2021 11 2021 3847409. Chen Doudou, Yang Tao, Zhu Siqu |
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