Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: PRDM5[original query] |
---|
Enrichment of pathogenic alleles in the brittle cornea gene, ZNF469, in keratoconus. Human molecular genetics 2014 Oct 23 (20): 5527-35. Lechner Judith, Porter Louise F, Rice Aine, Vitart Veronique, Armstrong David J, Schorderet Daniel F, Munier Francis L, Wright Alan F, Inglehearn Chris F, Black Graeme C, Simpson David A, Manson Forbes, Willoughby Colin |
Methylation and expression of the tumour suppressor, PRDM5, in colorectal cancer and polyp subgroups. BMC cancer 2015 15 20. Bond Catherine E, Bettington Mark L, Pearson Sally-Ann, McKeone Diane M, Leggett Barbara A, Whitehall Vicki L |
Mutation Survey of Candidate Genes and Genotype-Phenotype Analysis in 20 Southeastern Chinese Patients with Axenfeld-Rieger Syndrome. Current eye research 2018 6 43 (11): 1334-1341. Wang Xun, Liu Xing, Huang Liqin, Fang Shaohua, Jia Xiaoyun, Xiao Xueshan, Li Shiqiang, Guo Xiangmi |
Corneal Perforation After Corneal Cross-Linking in Keratoconus Associated With Potentially Pathogenic ZNF469 Mutations. Cornea 2019 5 38 (8): 1033-1039. Zhang Wenlin, Margines J Ben, Jacobs Deborah S, Rabinowitz Yaron S, Hanser Evelyn Maryam, Chauhan Tulika, Chung Doug, Bykhovskaya Yelena, Gaster Ronald N, Aldave Anthony |
Genotype-phenotype association of PITX2 and FOXC1 in Axenfeld-Rieger syndrome. Experimental eye research 2022 11 226 109307. Zhou Lin, Wang Xiaoli, An Jingqi, Zhang Yao, He Mengxia, Tang |
The Association of Novel Single-Nucleotide Variants in the Collagen Matrix-Encoding Gene PRDM5 with Aortic Aneurysmal Disease. Life (Basel, Switzerland) 2023 8 13 (8): . Peyton Moore, Adam Wolf, Mohanakrishnan Sathyamoort |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 29, 2024
- Content source: