对联是中国汉族传统文化瑰宝。
Is the Chinese traditional culture Chinese antithetical couplet treasure.
结论中国汉族儿童少年体质水平的地域差异较为明显。
Conclusion the district difference of constitution in Chinese Han nationality children is rather significant.
摘要：目的研究马来酸氟吡汀在中国汉族健康人体的药动学。
ABSTRACT: OBJECTIVE To investigate the pharmacokinetics of Flupirtine maleate in Chinese Han healthy volunteers.
秧歌舞是中国汉族的一种民间传统舞蹈，通常在北方省份表演。
汤圆是中国汉族的代表小吃之一，是元宵节最具有特色的食物。
As one of the representative delicacies in Han ethnic group, tangyuan is the most typical food for Lantern Festival.
结论中国汉族人atm基因的单核苷酸多态与白人存在较大差异。
Conclusion There are great differences in the SNPs of ATM gene between Chinese of Han ethnicity and Caucasian.
中秋节与春节、清明节、端午节并称为中国汉族的四大传统节日。
Mid-Autumn festival and Chinese New Year, Ching Ming festival, Dragon Boat festival and the four known as the Han Chinese traditional festivals.
结论：CACNA1H基因可能是中国汉族CAE的重要易感基因。
Conclusion CACNA1H is a susceptibility gene for CAE in the Chinese Han population.
本文的研究对象主要是来自中国东北农村的在韩离婚的中国汉族女性。
The main targets of this study are divorced Han-Chinese women in Korea originally from rural areas in northeastern China.
本研究将建立中国汉族正常人群TLR4基因座位的单核苷酸多态性图谱。
The aim of this study was to investigate the distribution of TLR4 polymorphisms in the general population of China.
目的：探讨中国汉族苗勒管发育异常患者中hoxa13基因是否存在突变。
Objective: To investigate whether HOXA13 gene mutation existed in Chinese Han patients with Mllerian duct abnormalities.
目的研究巯基嘌呤甲基转移酶（TPMT）活性在中国汉族和瑶族人群中的分布。
Objective To investigate thiopurine methyltransferase(TPMT) activity distribution in Chinese Han and Yao 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.
目的分析中国汉族寻常型白癜风的临床特征及家族遗传特征，探索其可能的遗传传递方式。
Objective to analyze the clinical features and to explore the potential mode of genetic transmission of vitiligo vulgaris in Chinese Han population.
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).
不幸的是，在过去几个星期里，加拿大的大众传播媒介一直对中国和中国汉族充满偏见指控。
Unfortunately, in the past weeks, the Canadian mass media have been full of biased allegations concerning China and ethic Han Chinese.
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.
这些样品来自生活在北京师范大学居民，他们自我确认在四个祖父母中有至少三个为中国汉族人。
These samples were collected from individuals living in the residential community at Beijing Normal University who were self-identified as having at least three out of four Han Chinese grandparents.
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.
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.
目的分析中国汉族骨髓供者的人类白细胞抗原(HLA)多态性，并寻找和鉴定新的HLA等位基因。
Objective To analyze human leukocyte antigen (HLA) polymorphism and search for new alleles in Chinese Han population bone marrow registry donors.
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.
方法样本为广州市、上海市、温州市、大连市、石家庄市五城市3 259名2~19岁的中国汉族城市儿童。
Methods The sample was 3 259 normal Han Chinese children aged 2~19 years from five cities of China.
目的探讨中国汉族人色氨酸羟化酶(TPH)基因A 218c多态性与单相抑郁症及其症状表型的遗传关联性。
Objective to investigate the association among tryptophan hydroxylase (TPH) gene A218C polymorphism, unipolar depression (UPD) and symptom phenotypes in han nationality of Chinese.
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.
结论上述SNP位点可能与中国汉族2型糖尿病相关，为进一步研究这一位点所在的基因与2型糖尿病的关系提供了理论依据。
ConclusionThe SNP may be associated with type 2 diabetes in the Han Chinese, which lays the basis for further study of the relation between the localized gene with type 2 diabetes.
结论上述SNP位点可能与中国汉族2型糖尿病相关，为进一步研究这一位点所在的基因与2型糖尿病的关系提供了理论依据。
ConclusionThe SNP may be associated with type 2 diabetes in the Han Chinese, which lays the basis for further study of the relation between the localized gene with type 2 diabetes.
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