Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Cataract and SOX2[original query] |
---|
Mutational screening of 10 genes in Chinese patients with microphthalmia and/or coloboma. Molecular vision 2009 15 . Zhang Xiaohui, Li Shiqiang, Xiao Xueshan, Jia Xiaoyun, Wang Panfeng, Shen Huangxuan, Guo Xiangming, Zhang Qingjio |
Genetic investigation of ocular developmental genes in 52 patients with anophthalmia/microphthalmia. Ophthalmic genetics 2018 Feb 1-9. Vidya Nair Gopinathan, Rajkumar Sankaranarayanan, Vasavada Abhay |
Common variants in SOX-2 and congenital cataract genes contribute to age-related nuclear cataract.
Communications biology 2020 Dec 3 (1): 755. Yonova-Doing Ekaterina, Zhao Wanting, Igo Robert P, Wang Chaolong, Sundaresan Periasamy, Lee Kristine E, Jun Gyungah R, Alves Alexessander Couto, Chai Xiaoran, Chan Anita S Y, Lee Mei Chin, Fong Allan, Tan Ava G, Khor Chiea Chuen, Chew Emily Y, Hysi Pirro G, Fan Qiao, Chua Jacqueline, Chung Jaeyoon, Liao Jiemin, Colijn Johanna M, Burdon Kathryn P, Fritsche Lars G, Swift Maria K, Hilmy Maryam H, Chee Miao Ling, Tedja Milly, Bonnemaijer Pieter W M, Gupta Preeti, Tan Queenie S, Li Zheng, Vithana Eranga N, Ravindran Ravilla D, Chee Soon-Phaik, Shi Yuan, Liu Wenting, Su Xinyi, Sim Xueling, Shen Yang, Wang Ya Xing, Li Hengtong, Tham Yih-Chung, Teo Yik Ying, Aung Tin, Small Kerrin S, Mitchell Paul, Jonas Jost B, Wong Tien Yin, Fletcher Astrid E, Klaver Caroline C W, Klein Barbara E K, Wang Jie Jin, Iyengar Sudha K, Hammond Christopher J, Cheng Ching- |
Novel SOX2 mutation in autosomal dominant cataract-microcornea syndrome. BMC ophthalmology 2022 2 22 (1): 70. Lin Zhi-Bo, Li Jin, Ye Lu, Sun Hai-Sen, Yu A-Yong, Chen Shi-Hao, Li Fen-F |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: