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   医学细胞遗传学 的翻译结果: 查询用时:0.293秒
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医学细胞遗传学
相关语句
  medical cytogenetics
     Objective To investigate the key feature of medical cytogenetics of genetic consultants in Putian, Fujian Province.
     目的 探讨福建莆田遗传咨询者的医学细胞遗传学主要特征。
短句来源
     The studies on SC may not only contribute to the knowledge of submicroscopic structure in meiosis but also has been widely used in the studies on eukaryotic chromosome rearrangement, medical cytogenetics and genetic toxicology.
     SC 的研究不但丰富了人们对减数分裂过程亚显微细节的了解,而且在真核生物染色体重排、医学细胞遗传学、遗传毒理学的研究中,也得到了普遍的重视和广泛的应用。
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  “医学细胞遗传学”译为未确定词的双语例句
     Objective To investigate the characteristics
     目的探讨不良孕产史医学细胞遗传学主要特征。
短句来源
     Objective: To investigate the main characteristic of medical genetics of Fujian Putian genetic counseling people .
     目的 :探讨福建莆田遗传咨询者的医学细胞遗传学主要特征。
短句来源
  相似匹配句对
     MEDICAL SCIENCE
     医学
短句来源
     Fan Zhongyan and Chinese Medicine
     范仲淹和医学
短句来源
     Objective To investigate the key feature of medical cytogenetics of genetic consultants in Putian, Fujian Province.
     目的 探讨福建莆田遗传咨询者的医学细胞遗传学主要特征。
短句来源
     Objective: To investigate the main characteristic of medical genetics of Fujian Putian genetic counseling people .
     目的 :探讨福建莆田遗传咨询者的医学细胞遗传学主要特征。
短句来源
     Molecular Cytogenetics of Chronic Lymphocytic Leukemia
     慢性淋巴细胞白血病的分子细胞遗传学
短句来源
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  medical cytogenetics
Dircs fill-service medical cytogenetics aboy; exnsive experine in human and mammlian Ksogenetic tu morcyp cs, chrmoso and DNAdamage.
      


730 cases of high risk chromosomal diseases were studied using medical genetic techniques. 63 of them were found to have abnormalities of chromosome number and structure, including 5 types of aberrations hitherto not yet reported in the world literoture.Chorionic villus samples were obtained from 4 of the fetuses in early pregnancies and their chromosomal karyotypes were fcund to be the same as those of their parental propositi. In 48 (76.2%) of the 63 cases, chromosomal aberrations were found to develop from...

730 cases of high risk chromosomal diseases were studied using medical genetic techniques. 63 of them were found to have abnormalities of chromosome number and structure, including 5 types of aberrations hitherto not yet reported in the world literoture.Chorionic villus samples were obtained from 4 of the fetuses in early pregnancies and their chromosomal karyotypes were fcund to be the same as those of their parental propositi. In 48 (76.2%) of the 63 cases, chromosomal aberrations were found to develop from abnormal zygotes or gametes, while in 11 (17.5%),abnormalities were inherited from their previous generations. The arigin of chromosomal diseases in the other 4 oases (6.3%) remained unknown.

本文应用医学细胞遗传学技术,检测高危染色体病730例,发现染色体数目和结构异常63例,其中5例异常核型为世界首报,4例之后代行绒毛检查,发现与先证者相同的异常核型。63例中,由于配子或合子发生的畸变有48例,占76.2%;由上代亲本遗传的11例,占17.5%;4例起源尚不能确定,占6.3%。

Objective To investigate the characteristics

目的探讨不良孕产史医学细胞遗传学主要特征。方法采用细胞遗传学方法对安徽地区201对有不良孕产史的夫妇进行外周血淋巴细胞检查。结果发现染色体异常核型29例,异常率为7.2%。其中常染色体异常16例,性染色体异常3例,染色体形态异常7例,标记染色体3例。结论染色体异常可能是流产、死胎、畸胎、畸形儿的原因之一;染色体的遗传多态性与疾病的关系应引起高度重视。

Objective To investigate the key feature of medical cytogenetics of genetic consultants in Putian, Fujian Province. Method Lymphocyte in blood was detected by cytogenetics method in 739 genetic consultants. Result Abnormality of chromatosome was found in 56 cases of 739 genetic consultants (7. 58%). Among them, abnormality of number or structure of autosome was found in 43(76.9% ), that of sex chromosome was found in 13 (23.1%). The most common abnormality was autosome's balanced translocation (in 19 cases,...

Objective To investigate the key feature of medical cytogenetics of genetic consultants in Putian, Fujian Province. Method Lymphocyte in blood was detected by cytogenetics method in 739 genetic consultants. Result Abnormality of chromatosome was found in 56 cases of 739 genetic consultants (7. 58%). Among them, abnormality of number or structure of autosome was found in 43(76.9% ), that of sex chromosome was found in 13 (23.1%). The most common abnormality was autosome's balanced translocation (in 19 cases, 33. 9% ) and 21 Trisomy( in 18 cases, 32.1 % ) .

目的 探讨福建莆田遗传咨询者的医学细胞遗传学主要特征。方法 采用细胞遗传学方法对739例遗传咨询者进行外周血淋巴细胞检查。结果 739例遗传咨询者中发现染色体异常56例,异常率为7.58%,其中常染色体数目结构异常43例,占76.9%,性染色体数目结构异常13例,占23.1%。尤以常染色体平衡易位(19例,占33.9%)、21三体型(18例,占32.1%)最多。结论 该研究用于临床可为遗传病寻找病因及明确诊断提供依据。

 
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