基因型频率

组间中医证型、基因型频率和等位基因频率分布使用χ2检验；

χ 2 test was used to analyze interclass of Chinese medicine syndrome , genotypic frequency and allele frequency distribution .

2型糖尿病心血管并发症风险因子与血管紧张素I转换酶等位基因和基因型频率的关联

Association of the risk factors of cardiovascular complication with the alleles and genotypic frequency of angiotensin I converting enzyme in type 2 diabetes mellitus

结果表明：三个群体的基因型频率与基因频率各不相同，皆以B基因频率最高，群体中BC型个体最多，C基因频率大于A基因频率；

Frequencies of genes and genotypes of each population were calculated respectively .

结果危重病组比正常对照组、非危重病组DD基因型频率高、II基因型频率低。

Results The DD genotype was significantly higher in critical group compared with the other two .

该位点各基因型频率和等位基因频率在哈萨克族高血压组和正常对照组的分布差异均有统计学意义（P0.05）。

The frequency of genotype in EH group was significantly different from that in NT group in Kazakh population ( P0.05 ) .

ACE基因型频率分布东方人与西方人不同。

The different frequencies of the ACE genotypes have been found between the East and the West .

CHD患者总体和分类型的基因型频率和等位基因频率与对照组相比差异无显著性；

No difference was observed in total and CHD type-dependent genotype distribution and allele frequency between patients and control .

在两种牦牛品系中，AA基因型频率最高，A等位基因频率均明显高于B等位基因频率。

Frequency of AA genotype is the highest , and that of A allele is obviously higher than that of B allele in two yak breeds .

统计学分析RA患者基因型频率、等位基因频率与各临床表型之间的关系。

Statistical analysis the relationship between patients with RA genotype frequencies , allele frequencies and the clinical phenotype . Results : 1 .

结果3个SNP基因型频率分布都符合Hardy-Weinberg平衡；

Results The genotype frequency distributions of three SNPs were all in Hardy-Weinberg equilibrium ;

ε3/ε4基因型频率ε4基因频率，AD组明显高于对照组（P<0.05）。

The ε 3 / ε 4 genotype frequence and ε 4 gene frequence of AD group are significantly higher than the comparison group ( P < 0.05 ) .

结果：满、汉、回三民族ABO血型的基因型频率和基因频率存在差异。

Results : There are differences in genotype frequency and gene frequency of ABO blood type among Man ? Han ?

结论1.脑梗死组与对照组CRP1059G/C基因型频率分布存在差异，C等位基因明显少于对照组。

There were statistically significant for CRP 1059G / C genotype frequencies between the patients with cerebral infarction and the healthy controls . The C allele in the patient with cerebral infarction was significantly less than the control group .

拟和优度X2检验（Goodness-of-fitChi-squaretest）分析对照组基因型频率的分布是否符合H-W平衡。

To analysis the genotype frequency distribution of the control group whether meets Hardy-Weinberg equilibrium by Goodness-of-fit Chi-square test . 5 .

有VMC病史的DCM患者中MCP-1-2518G/G基因型频率高。

The MCP-1-2518G / G genotype frequencies are higher in the DCM patients who have a VMC medical history . 3 .

结果：在不同种族中老年人群中II、ID、DD基因型频率分别为：美国白人：0.170、0.447、0.383；

Results : The occurrence frequency of ACE genotype in mid-aged population of different races was respectively as follow : II 0.170 , ID 0.447 , DD 0.383 in white American ;

三种基因型频率和等位基因频率在冠心病组和对照组间分布差异无显著性，血浆HDL含量在三种基因型中差异亦无显著性（P0.05）。

No significant difference of allele and genotype frequency of VNTR-ZNF between CHD and control groups . HDL plasma level did not show significant difference in three genotypes . 2 .

SPSS10.0软件包进行数据统计分析。结果：冠心病组与对照组的AA、AC基因型频率分别为0.853、0.147和0.877、0.123，两组之间AA、AC基因型频率比较无显著性差异（P>0.05）；

Statistical analyses were performed with the SPSS Software release 10.0.Results The genotype frequencies of AA and AC in the patients and control subjects were 0.853 、 0.147 and 0.877 、 0.123 respectively .

用Unphased软件进行各SNP位点基因型频率分布的组内检验。

Unphased program was used to analyze inside group genotype frequencies of the SNPs .

其中法洛氏四联症、主动脉缩窄、主动脉弓离断的TT基因型频率为29.7%~40.0%。

In patients with tetralogy of Fallot , coarctation of aorta or interruption of aortic arch , the frequency of the TT genotype varied between 29.7 % and 40.0 % .

获得了4个民族各约100名无关个体的PentaE位点的等位片段及基因型频率，共发现20个等位片段，其频率分布在0.0048~0.2396之间。

As a result , we found 20 alleles in the four nationalities with frequencies ranging from 0.0048 to 0.2396.The genotype frequencies of Penta E locus met Hardy-Weinberg equilibrium .

不同品种中OBR基因型频率和基因频率存在显著差异。

Moreover , the gene frequency and genotype frequency have significant differences in different breeds . 2 .

结果：冠心病组及其对照组中CC、CT、TT基因型频率分别为：75.78%、23.44%、0.78%和85.85%、14.15%、0%。

The frequencies of CC , CT and TT genotype in CHD group were 75.78 % , 23.44 % and 0.78 % respectively , while 85.85 % , 4.15 % and 0 % in normal group .

2型糖尿病合并肾病组TT基因型频率及T等位基因频率明显高于不伴有肾病的2型糖尿病组及正常对照组。

Elevated frequencies of TT genotype and T allele were observed in type 2 diabetes mellitus with nephropathy as compared with type 2 diabetes mellitus without nephropathy and normal control group .

2型DM合并冠心病（CHD）组ID基因型频率高于无CHD组，Ⅱ型基因频率低于无CHD组。

The frequency of ID genotype was significantly higher , while frequency of II genotype was lower in type 2 diabetic patients with coronary heart disease ( CHD ), when compared to those without CHD .

男性冠心病组的CG+GG基因型频率和G等位基因频率均显著低于男性对照组（18.0%，41.7%，P<0.05；0.090,0.208，P<0.05）；

CG + GG genotype frequencies and G allele gene frequency in the male CAHD group were significantly lower than those in the male control group ( 18.0 % , 41.7 % , P < 0.05 ; 0.090 , 0.208 , P < 0.05 );

IGT组、DM组GG基因型频率分别为8.7%和11.6%，显著高于NGT组（4.5%），GG基因型携带者脂联素水平显著降低。

The genotype GG frequencies in IGT and DM groups were 8.7 % and 11.6 % respectively , which were significantly higher than those in NGT group .

且伴血脂异常组DD基因型频率和D等位基因频率明显高于血脂正常组（P<005）。

Moreover , the frequency of DD genotype and D alleles in abnormity group were significantly higher than those in normal group of cholesterol and high-density lipoprotein ( P < 0.05 ) .

结果：（1）并发冠心病（CHD）组∈3／3基因型频率为52%，显著低于对照组76%（P＜0.01）；

The results showed : ( 1 ) the prevalence of genotype ∈ 3 / 3 was about 52 % in coronary atherosclerotic heart disease ( CHD ) group , which was significantly lower than 76 % in control ( P < 0 . 01 );

结果在阿尔茨海默病患者中GG，GC和CC基因型频率分别为16.39%，50.82%和32.79%；正常对照组中分别为26.03%，41.10%和32.87%。

Results Genotype frequency of GG , GC and CC were 16.39 % , 50.82 % and 32.79 % in patients with AD and 26.03 % , 41.10 % and 32.87 % in control subjects .