短臂

Genetic analysis with reciprocal crosses between gls and Kas plants indicated that gls possesses a recessive mutation in a single nucleotide locus.

遗传分析表明：gls突变体为单基因隐性突变；初步定位结果表明，GLS基因位于第四条染色体短臂上靠近0端的16万碱基附近区域。

The percentage distance (from the hybridization sites to centromeres) was(51.79±1.24)%.P5CS is widely present in monocot and dicot.

该探针定位于水稻第9染色体的短臂近端点处，信号点距着丝粒的相对距离为(51.79±1.24)%。P5CS基因广泛存在于单子叶和双子叶植物中。

FISH with the tomato 45S rDNA clone revealed very strong signal in the satellite on the short arm of chromosome 2 as well as weak signals in five CPD banded regions at pachytene or four pairs of CPD banded regions at metaphase.

用番茄的一个45S rDNA 克隆进行的荧光原位杂交，不仅在位于2号染色体短臂的随体上显示了强的杂交信号，而且在粗线期染色体的5个CPD带区或有丝分裂中期染色体的4对CPD带区显示了弱的杂交信号。

Bulked segregant analysis revealed that two primers, phi118 and phi 041, amplified polymorphic bands.

因此南方玉米锈病抗病基因定位于玉米10号染色体短臂上。

Short boom for tailplane with elevators and central fin and toed-in tip fins carrying rudders.

为电梯和中央鳍和机尾趾短臂在尖鳍舵进行。

Using a 3H-labelled 7.3kb fragment of 18S and 28S rRNA g enes as a probe and by chromosomal in situ hybridization,it was demonstrated tha t the autoradiographic silver grains to be located along entire p+ part of the m arker chromosome.

应用3H标记的7.3kb长的rRNA基因探针进行染色体原位杂交，自显影银颗粒沿整个p+区域分布，p+上的银颗粒数是正常近端着丝粒染色体短臂上银颗粒平均数的5倍。

A new electrostriction material strain measure method using optical lever has been proposed.Short arm senses micro strain at contact point,with the help of optical lever micro strain has been magnified to form a facula.The CCD camera samples the positions of facula and the micro displacement of contact point can be obtained.

提出利用光学杠杆测量电致伸缩材料性能的新方法，通过触点短臂传感微形变，并通过光学杠杆将微形变放大后形成光斑，利用CCD摄像头采集放大前后的光斑，通过对光斑图像进一步的处理可以得到微位移量，从而实现电致伸缩材料应变测量。

Nasopharyngeal carcinoma is an endemic cancer with particulargeographic and ethnic distribution within southern China, most frequently, withinGuangdong province. Etiologically, the disease involves multiple factors includinggenetic, Epstein-Barr viral, as well as other food and environmental factors.Cytogenetic studies have revealed that loss of heterozygosity on chromosome3p occurred in as many as 95 - 100％ of NPCs and 75％ of precancerous lesions,suggesting the presence of NPC associated tumor suppressor genes.

鼻咽癌(Nasopharyngeal carcinoma，NPC)是中国南部、尤其是广东省最为常见的恶性肿瘤，其发病与遗传因素、EB病毒感染、以及环境和饮食等多种因素有关。3号染色体短臂(3p)在高达95-100％的鼻咽癌和75％的癌前病变中发生杂合性丢失(Loss of heterozygosity，LOH)，提示3p缺失区域中存在与鼻咽癌发生密切相关的抑癌基因。

Two major genes controllinggrain hardness,Pina and Pinb, was located at the short arm of chromosome 5DS.

控制硬度的主效基因Pina 和Pinb 位于染色体5D 短臂上，软质对硬质为显性。

Background and Objective Pseudohypertrophic muscular dystrophy is a kind of lethal X-chain recessive inherited disease. The etiological factor is mainly due to gene mutation of Xp21 which induce the structural and functional abnormality of a kind of cell skeleton protein: dystrophin.

背景和目的假肥大型肌营养不良症(pseudohypertrophic muscular dystrophy，PMD)是一种常见的致死性X-连锁隐性遗传病，病因主要是由于X染色体短臂2区1带(Xp21)的基因突变而导致一种细胞骨架蛋白——抗肌萎缩蛋白的结构和功能异常所致。

But we don't care about Battlegrounds.

但我们并不在乎沙场中的显露。

Ah! don't mention it, the butcher's shop is a horror.

啊！不用提了。提到肉，真是糟透了。