Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Glaucoma and PAX6[original query] |
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Molecular basis of Peters anomaly in Saudi Arabia. Ophthalmic genetics 2004 12 25 (4): 257-70. Edward Deepak, Al Rajhi Ali, Lewis Richard Alan, Curry Stacey, Wang Zongren, Bejjani Bass |
Candidate gene study to investigate the genetic determinants of normal variation in central corneal thickness. Molecular vision 2010 16 562-9. Dimasi David P, Burdon Kathryn P, Hewitt Alex W, Savarirayan Ravi, Healey Paul R, Mitchell Paul, Mackey David A, Craig Jamie |
Mutational analysis and genotype-phenotype correlations in southern Indian patients with sporadic and familial aniridia. Molecular vision 2015 21 88-97. Dubey Sushil Kumar, Mahalaxmi Nagasubramanian, Vijayalakshmi Perumalsamy, Sundaresan Periasa |
Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract. Molecular medicine reports 2018 Sep . Lin Ying, Gao Hongbin, Zhu Yi, Chen Chuan, Li Tao, Liu Bingqian, Lyu Cancan, Huang Ying, Li Haichun, Wu Qingxiu, Jin Chenjin, Liang Xiaoling, Huang Xinhua, Lu L |
Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation. Molecular medicine reports 2018 6 18 (2): 1623-1627. Syrimis Andreas, Nicolaou Nayia, Alexandrou Angelos, Papaevripidou Ioannis, Nicolaou Michael, Loukianou Eleni, Sismani Carolina, Malas Stavros, Christophidou-Anastasiadou Violetta, Tanteles George |
Evaluation of the genetic association between early-onset primary angle-closure glaucoma and retinitis pigmentosa. Experimental eye research 2020 6 197 108118. Liu Xing, Li Jiali, Lin Shufen, Xiao Xueshan, Luo Jingyi, Wei Wei, Ling Yunlan, Fang Lei, Xiao Hui, Chen Liming, Huang Jingjing, Zhong Yimin, Zhang Qingjio |
Analysis of genotype-phenotype correlations in PAX6-associated aniridia. Journal of medical genetics 2020 5 58 (4): 270-274. Vasilyeva Tatyana A, Marakhonov Andrey V, Voskresenskaya Anna A, Kadyshev Vitaly V, Käsmann-Kellner Barbara, Sukhanova Natella V, Katargina Lyudmila A, Kutsev Sergey I, Zinchenko Rena |
Genetic analysis using next-generation sequencing and multiplex ligation probe amplification in Chinese aniridia patients. Orphanet journal of rare diseases 2024 10 19 (1): 394. Li Wang, Qingdan Xu, Wentao Wang, Xinghuai Sun, Yuhong Ch |
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