中国汉族人群细胞色素氧化酶CYP2C19表型存在多态性。
The Han nationality have the genotype polymorphism of cytochrome CYP2C19.
调查X染色体特异性位点DXS10 1在中国汉族人群的多态性。
Objective To investigate the polymorphism of DXS101 lucus in Chinese Han population.
目的考察性别对中国汉族人群细胞色素氧化酶cyp2c19遗传多态性的影响。
Aim to assess the effect of gender on genetic polymorphism of cytochrome CYP2C19 in Chinese population.
结论：在中国汉族人群中上前牙牙龈形态有2种类型，牙龈形态特征存在种族差异。
Conclusion There are 2 gingival morphological types of maxillary anterior tooth segment in Han Chinese. There is racial difference on gingival morphological characteristics.
目的：探讨中国汉族人群SLC6A4基因启动子区基因多态性与反社会人格障碍的关系。
Objective: To determine the association between the human SLC6A4 gene promoter polymorphism and the Chinese people with antisocial personality disorder(APD).
目的比较研究中国汉族人群HLAB40交叉反应组血清学分型与高分辨度dna分型结果。
Objective To compare the high resolution DNA typing method with serological method for HLA B40 cross reactive groups (CREG) typing in Chinese population.
目的：研究中国汉族人群中CYP3AP1基因型的分布特征及其与CYP3A活性的相关性。
AIM: To investigate the distribution of genotype of CYP3AP1 in Chinese Han population and the correlation with CYP3A activity.
目的：获得人类补体第六成分（C6）A413C单核苷酸多态性在中国汉族人群的分布特征。
Objective: To obtain the genotype frequencies and allelic frequencies of human complement C6 gene A413C single nucleotide polymorphism(SNP)in Hans.
目的研究中国汉族人群abo基因多态性，并将基因分型技术用于解决临床输注中血型血清学难题。
Objective to study ABO gene polymorphism of Chinese Han population and apply ABO genotyping technology to solve the serological problems of clinical transfusion.
目的：分析中国汉族人群血管紧张素原(agt)基因M 235t多态与原发性高血压合并脑梗死的关系。
Objective: To identify the association of M235T polymorphism of angiotensinogen (AGT) gene with essential hypertension complicated by brain infarction in Chinese Han population.
目的：直接采用基因测序分型方法对中华骨髓库标本进行检测，识别和确认中国汉族人群中新发现的等位基因。
OBJECTIVE: to detect the samples in Chinese Bone Marrow Bank by gene sequencing typing, and to identify novel allele in Chinese Han population.
方法：本研究为病例对照关联研究，包括245例溃疡性结肠炎患者和300例健康对照，全部为中国汉族人群。
METHODS: 245 UC patients and 300 healthy controls of Chinese Han descent were included in the case-control study.
目的探讨中国汉族人群5-羟色胺转运体基因连锁多态性区域（5-HTTLPR）与抑郁症及临床特征的相关性。
Objective To investigate the association of the polymorphism of serotonin transporter gene linked polymorphic(5-HTTLPR) region with depression and its clinical symptoms in the Han Chinese.
结论在中国汉族人群中GRIK2基因或邻近基因可能是精神分裂症和心境障碍的共同易患基因之一，并可能影响发病年龄。
Conclusion: the GRIK2 gene or neighboring gene may be one of common susceptible genes for schizophrenia and mood disorders in Chinese Han population, also may affect the age of onset.
结论在中国汉族人群中5-HTR6基因或邻近基因可能是精神分裂症易患基因之一，但可能不是心境障碍的易患基因。
Conclusion: The 5 - HTR 6 gene or neighboring gene may be one of common susceptible genes for schizophrenia, but not for mood disorders in Chinese Han population.
用本方法建立的中国汉族人群dyf15 5s 1基因座等位基因频率资料，为群体遗传学研究及法医学应用提供了基础资料。
The allele frequencies of DYF155S1 locus in Chinese Han population provided the basic data for the study of population genetics and forensic practices.
中国汉族人群Megsin基因变异与基因库中高加索人群存在较大差异，这可能与中国汉族人群对IgA肾病的高发病率具有重要联系。
There is much difference in genovariation of Megsin between Chinese Han population and Caucasian population , which may be associated with the high incidence of IgAN in Chinese Han population .
目的：探讨血管紧张素原基因A- 6g,T174M和G - 217 A位点多态性与中国汉族人群原发性高血压发病风险的关系。
OBJECTIVE: To investigate the association between the polymorphism of AGT gene at A-6G, T174M and G-217A sites and the risk for the attack of essential hypertension in Chinese Han population.
目的探讨中国汉族人群中5 -羟色胺(5 - HT) 2 A (5 -HT2A)受体基因多态性与阿尔茨海默病(AD)的相互关系。
Objective to detect the relation between 5-ht2a receptor gene polymorphism and Alzheimerdisease (AD) in Chinese.
本研究的目的是探讨GSTT1基因多态性与中国四川汉族人群肺癌遗传易感性的关系。
The objective of this study is to investigate the relationship between genetic polymorphism of GSTT1 and inherent susceptibility to lung cancer in Han population in Sichuan, China.
目的研究中国湖北汉族人群内皮素受体- B (EDNRB)基因的多态性与散发性先天性巨结肠症发病的关系。
Objective To analyze the relationship between polymorphisms of EDNRB gene and Hubei provincial patients of Han ethnicity with sporadic Hirschsprung disease (sHD).
目的探讨中国17个汉族人群3个STR基因座的遗传关系。
Objective To study the genetic relationship (3 short tandem repeat gene loci, abbreviated as 3 STR gene loci) in 17 groups of Han population in China.
结论IL 6基因- 572g等位基因可能是中国汉族人MI的易感因子，这可能与携带该等位基因的人群存在IL6水平的高表达有关。
Conclusion IL6 gene -572g allele may be a genetic susceptibility factor to MI attack of Chinese Hans population, and related to the high expression of IL6.
目的：了解基质金属蛋白酶9基因C1562T多态性与中国南方汉族人群不稳定型心绞痛易感性的关系。
AIM: to investigate the association between the matrix metalloproteinase-9 (MMP-9) gene C1562T polymorphism and the susceptibility to unstable angina pectoris (UAP) in Han population of South China.
目的获得并研究中国辽宁汉族人群D12S1686位点的基因频率。
Objective: To acquire and investigate the gene frequency of D12S1686 in Han ethnic population of Liaoning, China.
结论山西汉族人群HLA - A，-B，-DRB1基因具有中国北方汉族人群共有的遗传特征，但也有其自身的分布特点。
Conclusion the HLA-A, -b, -drb1 distribution in Shanxi han population shares some genetic characteristics with other han populations in northern part of China, but it exhibits its own characteristics.
目的探讨血管紧张素原AGT（M2 35T）基因多态性与中国四川籍汉族人群原发性高血压（EH）的关系。
Objective To investigate whether the angiotensinogen AGT(M235T) gene polymorphisms might be implicated in essential hypertension(EH) in Sichuan Hans population.
目的探讨血管紧张素原AGT（M2 35T）基因多态性与中国四川籍汉族人群原发性高血压（EH）的关系。
Objective To investigate whether the angiotensinogen AGT(M235T) gene polymorphisms might be implicated in essential hypertension(EH) in Sichuan Hans population.
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