Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: GDF6[original query] |
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Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate. European journal of human genetics : EJHG 2009 Feb 17 (2): 195-204. Chiquet Brett T, Hashmi Syed S, Henry Robin, Burt Amber, Mulliken John B, Stal Samuel, Bray Molly, Blanton Susan H, Hecht Jacqueline |
Mutational screening of CHX10, GDF6, OTX2, RAX and SOX2 genes in 50 unrelated microphthalmia-anophthalmia-coloboma (MAC) spectrum cases. The British journal of ophthalmology 2010 Aug 94 (8): 1100-4. Gonzalez-Rodriguez J, Pelcastre E L, Tovilla-Canales J L, Garcia-Ortiz J E, Amato-Almanza M, Villanueva-Mendoza C, Espinosa-Mattar Z, Zenteno J |
Mutational screening of 10 genes in Chinese patients with microphthalmia and/or coloboma. Molecular vision 2009 15 . Zhang Xiaohui, Li Shiqiang, Xiao Xueshan, Jia Xiaoyun, Wang Panfeng, Shen Huangxuan, Guo Xiangming, Zhang Qingjio |
Mutations in the LHX2 gene are not a frequent cause of micro/anophthalmia. Molecular vision 2010 16 2847-9. Desmaison Annaïck, Vigouroux Adeline, Rieubland Claudine, Peres Christine, Calvas Patrick, Chassaing Nicol |
Association of rs6982567 near GDF6 with neovascular age-related macular degeneration and polypoidal choroidal vasculopathy in a Han Chinese cohort. BMC ophthalmology 2014 14 140. Ji Yuying, Zhang Xiongze, Wu Kunfang, Su Yu, Li Meng, Zuo Chengguo, Wen Fe |
Mutation analysis of the genes associated with anterior segment dysgenesis, microcornea and microphthalmia in 257 patients with glaucoma. International journal of molecular medicine 2015 Oct 36 (4): 1111-7. Huang Xiaobo, Xiao Xueshan, Jia Xiaoyun, Li Shiqiang, Li Miaoling, Guo Xiangming, Liu Xing, Zhang Qingjio |
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 |
The mutational burden and oligogenic inheritance in Klippel-Feil syndrome. BMC musculoskeletal disorders 2020 Apr 21 (1): 220. Li Ziquan, Zhao Sen, Cai Siyi, Zhang Yuanqiang, Wang Lianlei, Niu Yuchen, Li Xiaoxin, Hu Jianhua, Chen Jingdan, Wang Shengru, Wang Huizi, Liu Gang, Tian Ye, Wu Zhihong, Zhang Terry Jianguo, , Wang Yipeng, Wu N |
[Clinical Characteristics and Genetic Analysis of Klippel-Feil Syndrome]. Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae 2021 3 43 (1): 25-31. Li Zi Quan, Geng Mo Zhao, Zhao Sen, Wu Zhi Hong, Zhang Jian Guo, Wu Nan, Wang Yi Pe |
Preoperative Serum Calcitonin Level and Ultrasonographic Characteristics Predict the Risk of Metastatic Medullary Thyroid Carcinoma: Functional Analysis of Calcitonin-Related Genes. Disease markers 2022 3 2022 9980185. Fan Yi, Xu Haishan, Lv Meiyan, Li Ni |
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- Page last updated:Apr 16, 2024
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