Table 2． Allele frequencies of CGG triplet repeat in VLDLR gene in CHD and control groups.

Roughly 25 % of people with European ancestry carry the allele of this gene.

在欧洲血统的人群中,大约25%的人携带这种基因的385A对位基因.

Homozygous and heterozygous carriers of the PTPN 22 1858 T allele had a decreased probability of remission.

PTPN221858T位点纯合子和杂合子达到缓解的可能性降低.

The dominant allele usually controls the normal form of the gene, while mutations are generally RECESSIVE.

显性基因通常控制基因的一般形式, 而突变通常是隐性的.

A Common Allele on Chromosome 9 Associated with Coronary Heart Disease.

9号染色体上一个常见的等位基因与冠心病有联系.

A Common Allele Chromosome 9 Associated with Disease.

在9号染色体螺旋上的一个普通的等位基因伴随着冠心病的发生.

Objective The objective was to establish the detecting method on allele frequencies bulk samples.

[目的]建立玉米群体混合样本等位基因及其频率的分析方法.

Only the patients carrying the allele M 235 T have correlation between genotype DD of ACE and preeclampsia.

ACE基因DD型与子痫前期的相关性限于携带有M235T等位基因的患者.

If the dog has two copies of the allele ( homozygous ), the dilution is much stronger.

如果有二个 ( 纯合 ), 这种淡化就十分强烈.

In some cases one allele is not completely dominant or recessive to another allele ( INCOMPLETE DOMINANCE ).

在一些类型中一个等位基因对另一个等位基因并不是完全显性或者隐性的 ( 不完全显性 ).

Now the variant of each gene is called an allele.

每一种基因的变化就叫做等位基因.

Usually only one of these, the dominant allele, is expressed in the phenotype.

通常只有其中的一个显性等位基因在表型中表达.

The mutation was confirmed by allele specific PCR ( ASPCR ).

应用等位基因特异性 PCR 验证测序所发现的突变.

The allele for blue eyes is recessive.

兰色眼睛的等位基因是隐性的.

Alleles of the apolipoprotein E gene have distinct neuroanatomic signatures , identifiable in childhood.

在儿童时期,载脂蛋白等位基因具有特殊的神经解剖学标记意义, 并可被识别.

An organism that has different alleles at a particular gene locus on homologous chromosomes.

杂合体在同源染色体的某一特定基因位点上有不同的等位基因的有机体.

Both of GPI and PGM, with 7 alleles , were the most variable loci.

其中变异最大的位点是GPI和PGM-.

They are formed by different alleles, and are a valuable tool for detecting genetic variation.

这归因于组成同功酶的亚单位及结构不同.

Some of these alleles are dominant, others recessive.

有些等位基因是显性的, 其他的是隐性的.

Some alleles are dominant over others.

一些等位基因比其他基因更具显性.

Risk from both alleles was confined to estrogen receptor-positive tumors.

两种等位基因引起的乳腺癌仅限于雌激素受体阳性肿瘤.