Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Cataract and PITX3[original query] |
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Identification of PITX3 mutations in individuals with various ocular developmental defects. Ophthalmic genetics 2018 2 39 (3): 314-320. Zazo Seco Celia, Plaisancié Julie, Lupasco Tatiana, Michot Caroline, Pechmeja Jacmine, Delanne Julian, Cottereau Edouard, Ayuso Carmen, Corton Marta, Calvas Patrick, Ragge Nicola, Chassaing Nicol |
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 |
Association of FOXE3-p.Ala170Ala and PITX3-p.Ile95Ile Polymorphisms with Congenital Cataract and Microphthalmia. Journal of ophthalmic & vision research 0 13 (4): 397-402. Vidya Nair Gopinathan, Ganatra Darshini, Vasavada Abhay R, Rajkumar Sankaranarayan |
PITX3 mutations associated with autosomal dominant congenital cataract in the Chinese population. Molecular medicine reports 2019 Feb . Wu Zehua, Meng Delong, Fang Chengbo, Li Jian, Zheng Xiujie, Lin Jiansuo, Zeng Haijiang, Lv Sihan, Zhang Zhenning, Luan Bing, Zhong Zilin, Chen Jianj |
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- Page last updated:Apr 16, 2024
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