Association Between DSCR1 Variations and Congenital Heart Disease Susceptibility

机译：DSCR1变异与先天性心脏病易感性之间的关联

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摘要

BackgroundThe objective of this study was aimed to detect the association of Down syndrome critical region 1 (DSCR1) gene polymorphisms (rs149048873 and rs143081213) and congenital heart disease (CHD) susceptibility.

机译：背景本研究的目的是检测唐氏综合症关键区域1（DSCR1）基因多态性（rs149048873和rs143081213）与先天性心脏病（CHD）易感性的关联。

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期刊名称 Medical Science Monitor : International Medical Journal of Experimental and Clinical Research
作者
Ren Yu Guo; Xiao Feng Li; Song Bai; Jian Guo; Nan Ding; Zhong Zhi Li;
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作者单位

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年(卷),期 2015(21),-1
年度 2015
页码 3536–3539
总页数 4
原文格式 PDF
正文语种
中图分类
关键词
Genes vif; Heart Defects Congenital; Polymorphism Single Nucleotide;

机译：基因;vif;先天性心脏病多态性;单核苷酸;

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专利

1. Association Between DSCR1 Variations and Congenital Heart Disease Susceptibility [J] . Ren Yu Guo, Xiao Feng Li, Song Bai, Medical science monitor : . 2015,第1期

机译：DSCR1变异与先天性心脏病易感性之间的关联
2. Congenital heart diseases and their association with the variant distribution features on susceptibility genes [J] . Su W., Zhu P., Wang R., Clinical Genetics: An International Journal of Genetics in Medicine . 2017,第3期

机译：先天性心脏病及其与易感基因变异分布特征的关联
3. Common Variations in BMP4 Confer Genetic Susceptibility to Sporadic Congenital Heart Disease in a Han Chinese Population [J] . Qian Bo, Mo Ran, Da Min, Pediatric cardiology . 2014,第8期

机译：BMP4的常见变异赋予中国汉族人群零星先天性心脏病遗传易感性
4. Total Variation Random Forest: Fully Automatic MRI Segmentation in Congenital Heart Diseases [C] . Anirban Mukhopadhyay International Workshop on Reconstruction and Analysis of Moving Body Organs . 2017

机译：总变异随机森林：先天性心脏病中的全自动MRI分段
5. Rare Copy Number Variations in Congenital Heart Disease Patients Identify New Genes in Left-Right Patterning [D] . Fakhro, Khalid Adnan 2011

机译：先天性心脏病患者的稀有拷贝数变异确定了左右模式中的新基因
6. Common Variation in ISL1 Confers Genetic Susceptibility for Human Congenital Heart Disease [O] . Kristen N. Stevens, Hakon Hakonarson, Cecilia E. Kim, 2010

机译：ISL1的常见变异赋予人类先天性心脏病遗传易感性
7. Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.: Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16. [O] . Cordell, Heather J, Bentham, Jamie, Topf, Ana, 2013

机译：多种先天性心脏病表型的全基因组关联研究确定了4p16染色体上房间隔缺损的易感基因座。

Association Between DSCR1 Variations and Congenital Heart Disease Susceptibility

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