chromosome的例句大全

Chromosome Observation and Karyotype Analysis of Rosa multiflovra var. Cathayensis

红刺玫染色体的观察和核型分析

Study on Tissue Culture and Technique of Chromosome Squashing in Dendrobium Nobile

春石斛组培快繁及染色体制片技术的研究

Gene mutations in human gene can cause various diseases. The human autosomal dominant brachydactyly type B ( BDB) and autosomal dominant polycystic kidney disease ( PKD) are due to gene mutation on chromosome.

人类基因组上基因的突变可以引起各种各样疾病的发生，人的常染色体显性的B型短指和常染色体显性的多囊肾综合症就是由于染色体上的基因突变引起的。

Started with ACO1 ( aconitase I), we got positive clone of ACO1 then obtained 16 clones by chromosome walking. After analysis fingerprinting of 16 BAC clones.

以离ID最近的ACO1（aconitase1，顺乌头酸酶）基因为起点，设计引物筛选含ACO1的BAC克隆，用染色体步行的方法得到16个BAC克隆。

Acrocentric chromosome ( ophthalmology) inability to focus on near objects.

近端点着丝粒染色体（眼）不能聚焦于近处物体。

However, there are two populations in which do not contain any acrocentric chromosome.

其中也有两个居群的染色体类型不含有近端部着丝粒染色体（st）。

The pathway of male sexual development in mammals is initiated by SRY, agene on the short arm boundary of Y chromosome.

哺乳动物中位于Y染色体短臂临界区域的SRY基因启动雄性性状的发育。

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。

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.

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。

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

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

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

Study on abnormality of sex chromosome in children

儿童性染色体异常的研究

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。

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。

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。

Unlike other sex chromosome aneuploidy, there are no general characteristic physical features for triple X patients.

与其他性染色体非整倍体不同，XXX核型的患者并没有显著的身体特征。

Similar to Mark W. The sex chromosome.

采用类似于Mark W.性染色体Z为中着丝粒染色体，W为近端着丝粒染色体。

Among 19 cases autosomal abnormal are 14 cases, sex chromosome abnormal are 5 cases.

其中，常染色体异常14例，性染色体异常5例。