1.
Three novel mutations of potassium channel HERG and SCN5A in Chinese families of congenital long QT syndromes
遗传性长QT综合征HERG基因及SCN5A基因新突变
2.
Dependence analysis between sudden manhood death syndrome and mutation of SCN5A;
青壮年猝死综合征与SCN5A基因突变的相关性
3.
Cardiac Sodium Channel Gene and Arrhythmogenic Cardiac Disorders;
心脏钠通道SCN5A基因突变与致心律失常性疾病
4.
The gene screening of SCN5A variation in Chinese patients with diagnostic and suspected Brugada syndrome
国人确诊及疑似Brugada综合征患者SCN5A基因变异筛查
5.
SCN5A mutations in a Chinese family with Atrioventricular Block and Dilated Cardiomyopathy
一个扩张型心肌病伴房室传导阻滞家系SCN5A基因的突变研究
6.
Effect of hypoxia on the activity of protein kinase A and the expression of SCN5A in cultured rat myocardial cells
低氧对大鼠心肌细胞蛋白激A活性与SCN5A基因表达的影响
7.
The screening of SCN5A mutations in sudden unexpected nocturnal death syndrome in Chinese Han nationality population
青壮年猝死综合征家系及散发病例SCN5A基因突变的检测
8.
Single Nucleotide Polymorphisms of SCN5A Gene in South Chinese Han Population and Their Correlation with Arrhythmias;
中国南方汉族人群SCN5A基因单核苷酸多态性分布特征及与心律失常的相关性研究
9.
Association between Single Nucleotide Polymorphisms of SCN5A Gene and Sick Sinus Syndrome
中国南方汉族人群中SCN5A基因多态位点和病态窦房结综合征的关联性
10.
Expression of voltage-gated sodium channel SCN5A/Nav1.5 in human ovarian cancer and its significance
电压门控钠通道SCN5A/Nav1.5在卵巢癌中的表达及意义
11.
extinguisher loci
消失基因座，绝灭基因座
12.
Of, relating to, produced by, or being genes or a gene.
基因的基因的，与基因有关的，基因产生的
13.
Genes are described as DOMINANT or RECESSIVE.
基因分为显性基因和隐性基因。
14.
hypomorphic allele
次等位因素对偶基因
15.
Studies on Polymorphism of Prolactin Receptor Gene and Follicle-Stimulating Hormone Beta Subunit Gene in Swine;
猪PRLR基因和FSHβ亚基基因多态性研究
16.
Research on Hte Microarray Based Gene Mining Algorithm;
基于基因表达谱的基因挖掘算法研究
17.
Human Genome Project,Post-genome Research and Gene Medicine --New Century of Diagnosis,Pharmaceutics and Therapy with Gene Technique;
人类基因组计划、后基因组研究与基因医学——基因诊断、基因制药与基因治疗的新世纪
18.
Genetic material produced by gene-splicing.
重组基因材料基因分割而产生的基因材料