染色的例句大全

The chromosome number and karyotype of Astragalus chinensis X.

本文首次报道了民和黄芪的染色体数目及核型.

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A new chromosome number and karyotype were found for the first time.

马鞍山居群的新染色体数目及核型均为首次报道.

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The karyotype and viral test were negative.

染色体和病毒测试结果阴性.

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This article reports chromosome number and karyotype analyais of Cyamopsis tetragonoloba and Calonyction muricotum.

本文报道了豆科瓜尔豆和旋花科跌打豆的染色体数目及核型.

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Objective : This article is to analyze the relationship between abnormal karyotype and male infertility.

目的 探讨男性不育与常染色体异常的关系.

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Karyotype analysis has been one important tool in studying silkworm heredity, variation and gene mapping.

家蚕染色体核型分析是研究家蚕遗传 、 变异和基因定位等的重要方法之一.

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They did a chromosome analysis of the tissue.

我做了组织染色体检查.

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Method: All the cases were undertaken karyotypic analysis, B-ultrasonic examination, semen examination and sexual hormone determination.

方法采用常规染色体核型分析、B超、精液检查及性激素测定。

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Genetic diagnosis of Down's syndrome using the STR of 21 chromosome

利用21号染色体上STR位点进行唐氏综合征基因诊断的研究

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Result There are 6 anomaly of chromatosome of fetus and 12 NTD in 4661 screened gravida, And we found the possibility of expulsion abnormal fetus was much higher in the high risk group than the lower risk group of Down's syndrome.

结果在筛查的4661名孕妇总检出6例胎儿染色体异常，12例神经管畸形（NTD），并发现唐氏综合征高风险孕妇娩出异常胎儿的可能性明显高于唐氏综合征低风险孕妇。

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Down syndrome ( DS) is one of the most common genetic diseases with mental retardation. DS has characteristic cognitive impairment phenotype because of its unique genotype.

唐氏综合征（Down syndrome，DS）是一种引起精神发育迟滞的最常见的常染色体遗传性疾病，由于其特殊的基因型导致了特殊的认知障碍表型。

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Objective: To investigate the expression level of genes located in chromosome 21 in the brain tissues of Down syndrome ( DS).

目的分析唐氏综合征（Down syndrome，DS）胎儿脑组织21号染色体（Chr21）基因的表达，探讨DS脑病变的分子机制。

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The observation of stained smears by microscopy showed cytomembrane ruptured, cytoplasm fluxed and cell necrosed.

细胞镜检及涂片染色发现癌细胞胞膜破裂、胞质外溢、细胞坏死。

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The number of AgNORs in VH , VC and SCC were 5.21±0.30 , 6.57±0.30 and 9.03±0.37 per cell, respectively.

核仁组成区嗜银蛋白染色数目在口腔上皮增生、状癌及鳞状细胞癌分别为每个细胞5.21±.30, 6.57±.30及9.03±.37.

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CGH analysis indicated copy number gains of 1 p 1, 1 q 2-4,2 p 1,2 q 1,5 p, 7 p 14,7 q 21,11 q 1,15 q 2,20 q and losses of 2 p 2,2 q 2,3 p , 4,9 p, 14,18, Xq.

比较基因组杂交结果得出染色体1p1、1q2-4 、 2p1、2q1、5p 、 7p14、7q21、11q1、15q2 、 20q扩增, 其中5p表现出高水平的扩增.

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Methods: We investigated chromosomal DNA copy number changes in 3 ESCC cell lines by comparative genomic hybridization ( CGH ).

方法: 采用比较基因组杂交法 ( CGH ) 分析3种ESCC细胞系的染色体DNA拷贝数改变情况.

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Among 43 cells with abnormal chromosomes , deletion, translocation , dicentrics , csb and inversion were demonstrated in 19,16,4 , 1 and 1 cells.

43个异常核型细胞中,缺失 、 易位、染色体断裂 、 双着丝粒、倒位各有19、16、4 、 1、1个细胞.

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Fullness tumor vascular and intense stain could be seen on DSA.

DSA显示瘤内血管丰富,呈血管团样,静脉期染色.

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DSA examination in 3 cases presented obvious staining of tumor.

行DSA检查3例,均显示明显的肿瘤染色.

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The technique of chromosome in situ hybridization ( CISH) has been extensively applied to genetics and breeding of higher plants.

染色体原位杂交技术近年发展较快，已广泛应用于植物遗传育种实践。

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