1、

Chromosome Diseases of Human ⅱ. Sex Chromosome Diseases

人类染色体疾病

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2、

Sex chromosome abnormalities and analysis of the relationship between male infertility

性染色体异常与男性不育的关系分析

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Non-gonadal defect and abnormal sex chromosome syndrome

无性腺缺陷-性染色体异常综合征

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4、

The sex chromosome is XY.

性染色体为XY。

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5、

Conclusion Sex chromosome aberration is the most important cause that results in sex differential distortion.

结论性染色体异常是导致性分化异常的重要原因之一。

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6、

The No. 5 is sex chromosome ( ZW type).

5为异型性染色体(ZW型);

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7、

Mechanisms of the sex chromosome aberration causing abnomal sex development were discussed.

在这些研究结果的基础上,本文对由于性染色体畸变而导致的性别发育异常的机制进行了分析和讨论。

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8、

Based on the model of XY type sex chromosome, the entropy variation regularity of sex linked population equilibrium was studied by using the information theory method.

以XY型性染色体为模型,运用信息论方法研究了性连锁群体平衡的熵变规律。

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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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10、

Study on abnormality of sex chromosome in children

儿童性染色体异常的研究

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11、

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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12、

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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13、

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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14、

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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15、

This make dead cotton more receptive to dyes.

这样有助于棉花更易接受染色.

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16、

The process required optimized process and machinery technologies as well as made-to-measure development a special auxiliary.

这项工艺要求优化的工艺和机械技术以及一种用于等温染色的特殊助剂.

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17、

The cell begins reduction by first separating its DNA chromosomes.

细胞通过首次DNA染色体分离开始减数分裂.

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18、

Multiple osteochondromas can occur either spontaneously an autosomal dominant disorder known as hereditary multiple exostoses.

多发骨软骨瘤可能是自发,也可能是常染色体显性遗传疾病—遗传性多发性外生骨疣病的表现.

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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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20、

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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