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兰色眼睛的等位基因是隐性的。The allele for blue eyes is recessive.
蓝色眼睛的等位基因是隐性的。The allele for blue eyes is recessive.
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而在蒙古羊群体中未检测到该突变。No B allele was detected in the Mongolia sheep.
每一种基因的变化就叫做等位基因。Now the variant of each gene is called an allele.
野生型等位基因对应形成中等长度的籽粒。The wild-type allele corresponds to medium grain.
此基因的等位基因有这一系列的可能性。Instead, each allele of the gene sets out a series of probabilities.
亚洲人身上有非洲人没有的等位基因HLA-A*11。The allele HLA-A*11 also appears in modern Asians, but not in Africans.
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DR基因多态性与UC的临床分型密切相关。HLA-DR allele polymorphism is associated with clinical classification of UC.
例如,受铭印基因当中,遭到消音的对偶基因上头,绝大多数都具有高度的甲基化。The silent allele of an imprinted gene is almost always highly methylated , for example.
表2.冠心病组与对照组低密度脂蛋白受体基因CGG重复等位基因频率分布。Table2. Allele frequencies of CGG triplet repeat in VLDLR gene in CHD and control groups.
NAT2表型和等位基因分布在不同的民族和地域之间具有显著性差异。Both NAT2 phenotype and allele are remarkably different in different nationality and zone.
口语用法基因通常指的是科学发展观的一个等位基因。The colloquial usage of the term gene often refers to the scientific concept of an allele.
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先证者的父母必定是杂合子,各携带一个突变等位基因。The parents of a proband are obligate heterozygotes and therefore carry one mutant allele.
否则,即使只有一个等位错配的基因,连接反应也不会发生。Otherwise even when there is an allele mismatch between them, no ligation would take place.
计算等位基因频率、遗传距离,构建系统发生树。Allele frequency and genetic distance were calculated and phylogenetic tree was constructed.
目的调查福建汉族人群HLA-DRB1等位基因的多态性。Objective To investigate the HLA-DRB1 allele polymorphism in Fujian Han nationality population.
该基因将世界分成两个群体——该基因携带者和非携带者。The risk gene divides the world into two camps ―those who have the FTO allele and those who don't.
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这种风险基因将会把世界分为两大阵营——脂肪量和肥胖相关的变种基因携带者和未携带者。The risk gene divides the world into two camps ― those who have the FTO allele and those who don't.
分析比较此多态位点的基因型和等位基因频率在不同人群中分布的差异。The difference of genotype and the variation of allele frequencies were analyzed by Chi-square test.
结论—这些实验结果证实了显性抑制的ALK2变异体-L343P等位基因存在于房室间隔缺损患者中。Conclusion—These data identify the dominant-negative allele ALK2 L343P in a patient with AVS defects.