他和同事测定了8000多条鳕鱼的基因型，研究两个鱼群中不同版本的基因，或者说等位基因的频率在1994年至2003年间是如何变化的。
He and his colleagues genotyped more than 8000 fish to find out how the frequency of different versions of the gene, or alleles, changed in the two populations between 1994 and 2003.
研究小组发现，携带一个或两个这种名为“334型等位基因变种”的男性与没有这种基因变种的男性相比，对待婚姻或感情的态度有所不同。
The team found that men who carry one or two copies of a variant of the gene often behave differently in relationships than men who lack the gene variant, called allele 334.
瓦卢姆说：“与不携带‘334型等位基因变种’男性的妻子相比，携带一个或两个此种基因变体男性的妻子对婚姻的满意度平均较低。”
"Women married to men who carry one or two copies of allele 334 were, on average, less satisfied with their relationship than women married to men who didn't carry this allele, " Walum said.
不同基因型决定相同表型的现象。参见等位基因异质性、临床异质性和基因座异质性。
Genetic lethal --- A mutant allele or genetically determined trait that leads to failure to reproduce, although not necessarily to death prior to reproduction.
目的分析江西汉族骨髓供者人类白细胞抗原(HLA)- A、B、DRB1等位基因频率和HLA单倍型频率。
Objective To analyse the human leukocyte antigen (HLA) -a, b, DRB1 allele and haplotype frequencies in Jiangxi Chinese Han unrelated bone marrow donors.
目的对原发性高血压患者进行HLA -DQA1等位基因的分型，分析高血压病患者的遗传易感性。
Objective To analyse the hereditary susceptibility by genotyping of HLA DQA1 alleles in essential hypertensives.
方法运用聚合酶链反应-序列特异性引物（PCR-SSP）法，对38例山东汉族人GPP与94例健康对照进行HLA-DQB1等位基因分型。
Methods The distributing frequencies of HLA-DQB1 alleles were detected with polymerase chain reaction-sequence specific primers (PCR-SSP) in 38 GPP patients and 94 healthy subjects from Shandong.
结论：1型糖尿病和腹腔疾病分享共同的遗传易感性等位基因。
Conclusions: a genetic susceptibility to both type 1 diabetes and celiac disease shares common alleles.
结论携带RHD1227A等位基因的中国汉族D放散型个体红细胞膜可能表达基本完整D抗原。
Conclusions The red blood cells may have grossly complete D antigen expression in the DEL individuals carrying RHD1227A alleles.
结论本方法快速、简便、精确，可为肾移植中DR 4阳性供受者HLADRB1等位基因的配型提供可靠的方法。
Conclusion This method is rapid, simple and accurate and is useful for matching type of HLA DRB1 alleles of DR4 positive donor and recipient in renal allograft.
所以，有些人拥有两个短型等位基因，有些人拥有两个长型等位基因，剩下的则长型短型各一个。
So some have two short alleles, some have two long ones, and the rest have one of each.
目的研究急性运动性轴索型神经病（AMAN）的易感性与HLA A、B等位基因分型的关系，探讨AMAN患者免疫遗传的特点。
Objective To explore the relations between susceptibility to AMAN and frequencies of HLA A? B alleles, and to identify the characteristics of the patients with AMAN in immunogenetics.
但该位点的基因型频率和等位基因频率在三组之间均没有统计学差异。
However, genotype and allele frequencies of this site showed no significant difference among different groups.
中国汉族健康群体与高加索、德国及日本报道的人群多巴胺D1受体-48A/G等位基因分布和基因型的分布不同。
The distributions of dopamine D1 receptor -48A/G allele and genotype in healthy Chinese Han population are different from those in Caucasian, German and Japanese.
结果：冠心病组HL–514C/T位点基因型和等位基因的分布与对照组相比，差异有统计学意义（P<0.05）。
Results:The genotype and allele distribution of HL-514C/T polymorphism were significantly different between the whole CHD group and control group(P<0.05).
多元回归分析显示，高胆固醇酯转运蛋白水平和B1等位基因是2型糖尿病大血管病变的危险因素。
Multiple logistic analysis showed that the serum CETP and its B1 allele were the important risk factors of type 2 diabetic macroangiopathy.
PON1QR192基因型和等位基因频率分布在脑出血组与对照组间差异无显著性意义；
There was no significant difference in PON1Q/R192 allele and genotype distribution between the cerebral hemorrhage group and the control group.
比较各组基因型及等位基因频率分布。
ApoE genotypes and alleles frequencies were compared among three groups.
临床糖尿病肾病组的TC／CC基因型频率和-429C等位基因频率显著低于其它各组；
The frequencies of genotype TC/CC and -429C allele in group CDN were lower than other groups.
ACE基因dd型与子痫前期的相关性限于携带有m 235t等位基因的患者。
Only the patients carrying the allele M235T have correlation between genotype DD of ACE and preeclampsia.
由基因型频率计算等位基因频率。
The allelomorph frequencies were calculated with genotype frequencies.
目的探讨白癜风中医证型与人类白细胞抗原（HLA）-DQB1等位基因的相关性及对白癜风易感性的影响。
Objective It is to discuss the correlation between syndrome type of traditional Chinese medicine of vitiligo and HLA-DQB1 alleles, and their effects on susceptibility of vitiligo.
STR分型表现为杂合子或纯合子的等位基因用此方法测序都得到了清晰的信号。
Good signals had been obtained, no matter the alleles showed homozygotes or heterozygotes on STR genotyping.
目的探讨HLA - DQA1和DQB1等位基因与汉族人寻常型银屑病遗传易感性。
Objective to explore HLA-DQA1 and DQB1 alleles in their association with genetic susceptibility to psoriasis vulgaris (PV) in Han Chinese.
将存活个体和死亡个体分别进行等位酶分析以确定每个个体的基因型。
The allozyme analysis was then employed to determine the number of each genotype for both surviving and dead individuals.
目的研究载脂蛋白E基因多态性与脑梗死的关系及不同等位基因型血脂水平的特点。
Objective To study the relationship between gene polymorphism of apolipoprotein E and cerebral infarction(CI) and the characteristics of the serum lipid level with different genotypes.
目的研究中国人群中载脂蛋白E等位基因型与阿尔茨海默病的关联。
Objective To analyse the association of apolipoprotein E genotypes with Alzheimer' s disease in Chinese population.
Arg16等位基因纯合型的孩子同时家中有2个甚至更多的吸烟者的有多5倍的终生喘鸣的风险。
Children who were homozygous for the Arg16 allele and were exposed to two or more smokers had a 5-fold increased risk of lifetime wheeze.
Arg16等位基因纯合型的孩子同时家中有2个甚至更多的吸烟者的有多5倍的终生喘鸣的风险。
Children who were homozygous for the Arg16 allele and were exposed to two or more smokers had a 5-fold increased risk of lifetime wheeze.
应用推荐