chromosomal的例句大全

Objective : To analyze the correlation between karyotypes and clinical presentations of patients with chromosomal abnormality.

目的研究染色体异常与临床疾病发生之间的关系.

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The complex chromosomal rearrangement could be transmitted stably in the family, but still the carriers could give birth to a healthy baby by chance.

染色体复杂重排仍可在家庭中稳定传递，携带者具有出生正常后代的可能。

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Objective To detect the characteristic chromosomal changes in Chinese children with infantile autism.

目的检测中国儿童孤独症患者的特征性染色体改变.

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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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Molecular Cloning, Chromosomal Localization, and Expression Pattern of Porcine Arf Gene Family

猪Arf家族基因的克隆、定位及组织表达谱分析

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Objective: Effects of the preservative Potassium sorbate on micronuclei and chromosomal aberrations in root tip cells of Vicia faba and inhibition of β-carotene 、 vitamin B2 and vitamin C on genetic toxicity induced by Potassium sorbate were studied.

目的研究防腐剂山梨酸钾对蚕豆根尖细胞微核和染色体畸变的影响及β胡萝卜素、维生素B2和维生素C对山梨酸钾遗传毒性的抑制作用。

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The micronucleus frequency may be causally related to radiation-induced genomic instability which is expressed as chromosomal damage leading to micronuclei.

表明微核发生率与染色体损伤程度存在剂量相关性，微核检测技术可以用于生物效应表现为染色体损伤的辐射诱导基因组不稳定性的研究。

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Study on polymorphism of XPD gene and radiation-induced chromosomal damage

XPD基因多态性与辐射致染色体损伤关系

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Case of partial mole was triploid, 69, XXY and with a chromosomal contribution from the female gamete.

1例部分性葡萄胎为三倍体，69，XXY，来源为双精子与一卵子结合而成。文章对完全性葡萄胎和部分性葡萄胎的发生来源做了简要的讨论。

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Results: According to the patients ′ cytogenetics examination, it is found there are 11 cases abnormal chromosomal karyotypes, including 6 cases of chromosome translocation, 2 cases of 47, XXY, 3 cases of big Y chromosome.

结果发现异常核型11例，其中染色体易位6例、2例47，XXY、3例大Y染色体。

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Mitochondrial Eve is the female counterpart of the Y-chromosomal Adam, the patrilinear most recent common ancestor.

线粒体夏娃是人类最亲近的共同父系祖先——Y染色体亚当的女性配偶.

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The following images represent a rare chromosomal anomaly diagnosed at 26 weeks of pregnancy.

这是一例孕26周诊断的罕见的染色体异常.

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Among them, there were 9 cases of abnormal chromosomal number, 4 cases of abnormal structure aberration and 2 cases of number anomalies of sex chromosome.

其中常染色体数目异常9例，结构异常4例，性染色体数目异常2例。

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There were 61 cases of sex chromosome abnormality accounting for 37.20% in the chromosomal abnormal karyotype;

性染色体异常61例，占染色体异常核型的37.20%；

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Study on chromosomal centromeric dots in couples with spontaneous abortion

自然流产夫妇染色体着丝粒点的研究

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The present statistical study indicates that major chromosomal anomalies to be involved in repeated reproductive wastage.

目前的统计研究表明,主要的染色体异常似乎参与了流产机制.

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The common patrilineal ancestor of all humans alive today has been dubbed Y-chromosomal Adam.

今天所有人类的共同父系祖先已经被授予了Y染色体亚当的称号.

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The incidences of fetal chromosomal anomaly and selected adverse pregnancy outcomes were correlated to PAPP-A concentration.

选择胎儿染色体异常作回顾件分析异常妊娠结局的发生率与PAPP -A 浓度的关系.

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Individuals who have deletions in this chromosomal region a high likelihood of developing autism.

个人谁有缺失的染色体区域在这个有很高的可能性发展中国家孤独症.

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Isolation and Chromosomal Localization of ZFX Homologue in Genome of Rice Field Eel ( Monopterus albus Zuiew )

ZFX基因同源序列在黄鳝基因组中的检出及其染色体定位 ( 英文 )

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