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浏览/检索结果: 共4条，第1-4条 帮助 已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择作者升序作者降序题名升序题名降序发表日期升序发表日期降序提交时间升序提交时间降序 DNA methylation status of TBX20 in patients with tetralogy of Fallot 期刊论文 BMC MEDICAL GENOMICS, 2019, 卷号: 12 作者:  Gong, Juan;  Sheng, Wei;  Ma, Duan;  Huang, Guoying;  Liu, Fang 收藏  |  浏览/下载：6/0  |  提交时间：2019/12/05 DNA methylation  TBX20 gene  Sp1 transcription factor  Tetralogy of Fallot   Association between the promoter methylation of the TBX20 gene and tetralogy of fallot 期刊论文 SCANDINAVIAN CARDIOVASCULAR JOURNAL, 2018, 卷号: 52, 期号: 5, 页码: 287-291 作者:  Yang, Xiaofei;  Kong, Qingyu;  Li, Zhenghao;  Xu, Min;  Cai, Zhifeng 收藏  |  浏览/下载：2/0  |  提交时间：2019/12/11 TBX20  gene  methylation  tetralogy of Fallot  promoter   Relationship between TBX20 gene polymorphism and congenital heart disease 期刊论文 GENETICS AND MOLECULAR RESEARCH, 2016, 卷号: 15, 期号: 2 作者:  Yang, X. F.;  Zhang, Y. F.;  Zhao, C. F.;  Liu, M. M.;  Si, J. P. 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/17 TBX20 transcription factor  Gene polymorphism  Allele  Congenital heart  disease  Single nucleotide polymorphism loci  Genotype frequency   A novel variant in TBX20 (p.D176N) identified by whole-exome sequencing in combination with a congenital heart disease related gene filter is associated with familial atrial septal defect 期刊论文 Journal of Zhejiang University. Science B, Biomedicine & Biotechnology, 2014, 卷号: 15, 期号: 9, 页码: 830-837 作者:  Liu Jijia;  Fan Liangliang;  Chen Jinlan;  Tan Zhiping;  Yang Yifeng 收藏  |  浏览/下载：5/0  |  提交时间：2019/12/03 Congenital heart disease (CHD)  Atrial septal defect (ASD)  Whole-exome sequencing  CHD-related gene filter  TBX20