Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Retinal Detachment and FBN1[original query] |
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Marfan syndrome: ocular findings and novel mutations-in pursuit of genotype-phenotype associations. Canadian journal of ophthalmology. Journal canadien d'ophtalmologie 2016 Apr 51 (2): 113-8. Latasiewicz Marta, Fontecilla Christian, Millá Elena, Sánchez Auro |
Genotype variant screening and phenotypic analysis of FBN1 in Chinese patients with isolated ectopia lentis. Molecular medicine reports 2021 2 23 (4): . Zhou Yijing, Guo Dongwei, Cao Qianzhong, Zhang Xinyu, Jin Guangming, Zheng Danyi |
[Correlation of posterior segment lesions with anterior segment biometric parameters and FBN1 genotype in patients with Marfan syndrome]. [Zhonghua yan ke za zhi] Chinese journal of ophthalmology 2024 7 60 (7): 601-610. Y Liu, T H Chen, Y X Jia |
Clinical and genetic risk factors underlying severe consequence identified in 75 families with unilateral high myopia. Journal of translational medicine 2024 1 22 (1): 75. Yi Jiang, Xueshan Xiao, Wenmin Sun, Yingwei Wang, Shiqiang Li, Xiaoyun Jia, Panfeng Wang, J Fielding Hejtmancik, Qingjiong Zha |
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