Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Microcephaly and KIF11[original query] |
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Identification of novel KIF11 mutations in patients with familial exudative vitreoretinopathy and a phenotypic analysis. Scientific reports 2016 6 26564. Li Jia-Kai, Fei Ping, Li Yian, Huang Qiu-Jing, Zhang Qi, Zhang Xiang, Rao Yu-Qing, Li Jing, Zhao Peiqu |
Novel variants in familial exudative vitreoretinopathy patients with KIF11 mutations and the Genotype-Phenotype correlation. Experimental eye research 2020 7 199 108165. Chen Chonglin, Sun Limei, Li Songshan, Huang Li, Zhang Ting, Wang Zhirong, Yu Bilin, Luo Xiaoling, Ding Xiaoy |
Genotype Phenotype Correlation and Variability in Microcephaly Associated With Chorioretinopathy or Familial Exudative Vitreoretinopathy. Investigative ophthalmology & visual science 2020 11 61 (13): 2. Shurygina Maria F, Simonett Joseph M, Parker Maria A, Mitchell Amanda, Grigorian Florin, Lifton Jacob, Nagiel Aaron, Shpak Alexander A, Dadali Elena L, Mishina Irina A, Weleber Richard G, Yang Paul, Pennesi Mark |
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- Page last updated:Apr 16, 2024
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