chromosome的例句大全

This is the first study of the genetic causes of infertility that links a particular sex chromosome meiosis-specific gene to sterility.

这是关于与某个特定性染色体连锁，与减数分裂和不育症有关的基因导致不育的首个研究。

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Study on abnormality of sex chromosome in children

儿童性染色体异常的研究

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The Technical Research of Fluorescence in Situ Hybridization for Detection of Fetal Sex Chromosome on Uncultured Amniotic Fluid Cells in Second Trimester

荧光原位杂交技术用于孕中期未培养羊水细胞胎儿性染色体检测的研究

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Research Progress on Sex Chromosome Evolution in Dioecious Plants

雌雄异株植物性染色体演化研究进展

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A Study of Sex Chromosome in Carassius auratus by BrdU-Hoechst 33258-Giemsa Technique

应用BrdU-Hoechst33258-Giemsa技术对鲫鱼性染色体的研究

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Breeders need to be aware of the sex linked diseases, which is an abnormal gene contained in X chromosome.

繁殖者需要了解到的性状疾病，那就是X染色体中存在着不正常的基因。

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Objective : To analyze the connection between abnormal chromosome karyotype and sexual abnormality.

目的分析性发育异常与染色体异常的关系.

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In 215 Azoospermia, chromosome abnormal rate was 12.09%.

无精子症215例，异常26例（异常率12.09%）；

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Conclusion: Chromosome abnormality is a major genetic factor that causes abortion, amenia and dysgenitalis, and should be highly emphasized by clinicians.

结论染色体异常是导致流产、闭经、性发育异常的重要遗传因素，应引起临床医师的高度重视。

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Methods: To analyze the chromosome karyotypes of circular lymphocytes in 61 patients with primary amenia.

方法分析61例原发闭经患者外周血淋巴细胞染色体核型。

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Objective: To analyze abnormal chromosome karyotype and pathogenesis of primary amenia.

前言：目的分析原发闭经患者染色体核型与病因。

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Chromosome count showed that the plants, containing non tetraploid cells besides amphidiploid, were chimeras.

染色体检查发现，除了四倍体之外，还存在其它倍性的细胞，呈嵌合体状态。

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The Analysis of Chromosome Karyotypes and Taxonomic Relationships of Amygdalus Plants

桃属植物染色体核型及种间亲缘关系分析

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Construction of a Bacterial Artificial Chromosome Library of Cotton Cultivars

棉花品种细菌人工染色体（BAC）文库的构建

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Optimized Method for Construction of Bacterial Artificial Chromosome Library in Cotton

棉花细菌人工染色体文库构建的方法优化

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ZResults There was positive correlation between micronuclei as well as between chromosome aberration and cumulative dose.

结果染色体畸变率和淋巴细胞微核检出率与接触射线累积剂量呈正相关.

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Chromosome aberration types and levels of sex hormones in 630 patients with azoospermia

630例无精子症患者染色体畸变及性激素水平

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The numbers of MiHAs are huge and their coding genes are in the hole genome, including autosome, Y chromosome and mitochondrial gene.

MiHAs数量庞大，其编码基因分布于整个基因组，包括常染色体、Y染色体、线粒体DNA，现已发现的人类MiHAs有十几种。

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Based on the hereditary properties of NPV resistance, a hypothesis was proposed and confirmed that the resistance is controlled by NN main gene on an autosome and Z+ Z+ minor genes on the sex chromosome.

根据其遗传规律的特殊性，提出常染色体上NN主基因和性染色体上Z+Z+修饰基因控制假设，并得到试验验证。

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And there are 34 cases of autosome abnormalities which is 25% in all examiners and 46% in chromosome abnormalities.

常染色体异常34例，占全部被检者25%，占异常核型46%。

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