Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Cataract and CRYBB2[original query] |
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Whole Exome Sequencing Reveals a Mutation in CRYBB2 in a Large Mexican Family with Autosomal Dominant Pulverulent Cataract. Molecular syndromology 2016 May 7 (2): 87-92. Messina-Baas Olga, Gonzalez-Garay Manuel L, González-Huerta Luz M, Toral-López Jaime, Cuevas-Covarrubias Sergio |
High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia. G3 (Bethesda, Md.) 2017 8 7 (10): 3257-3268. Javadiyan Shari, Craig Jamie E, Souzeau Emmanuelle, Sharma Shiwani, Lower Karen M, Mackey David A, Staffieri Sandra E, Elder James E, Taranath Deepa, Straga Tania, Black Joanna, Pater John, Casey Theresa, Hewitt Alex W, Burdon Kathryn |
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 |
Deciphering the association of intronic single nucleotide polymorphisms of crystallin gene family with congenital cataract. Indian journal of ophthalmology 2021 Aug 69 (8): 2064-2070. Nair Vidya, Sankaranarayanan Rajkumar, Vasavada Abhay Raghuka |
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? |
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- Page last updated:Apr 29, 2024
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