目的：介绍短串联重复序列在医学中的应用。
Objective: To introduce the application of short tandem repeats in medicine.
结果：短串联重复序列已广泛应用于医学临床和研究。
Results:Short tandem repeats were used widely for the study and clinic in medicine.
结论：短串联重复序列是目前医学中应用的主要遗传标记。
Conclusions: Short tandem repeats are the major genetic markers used in medicine.
短串联重复序列(STR)作为第二代遗传标记，广泛的分布于人类基因组中。
As the second generation of genetic marks, short tandem repeats are extensively distributed in human genome.
短串联重复（STR）是Y染色体NRY区的多态性遗传标记的一种，又称微卫星。
Short tandem repeat ( STR) is one of the genetic polymorphic markers within the NRY region in Chromosome Y, which is also called microsatellite.
所有位点都包含称为短串联重复序列的遗传结点，在结点里一个碱基对模式一遍遍重复出现。
All of these regions contain genetic stutters called short tandem repeats, in which a pattern of base pairs repeats itself over and over.
目的用短串联重复位点检测方法，评价组织工程化肌腱临床应用修复喙锁韧带损伤的效果。
Objective To evaluate the result of clinical application in the repair of coracoclavicular ligament injury by tissue engineered tendon using the technique of short tandem repeat loci examination.
目的：获得X染色体短串联重复序列DXS16遗传多态性在河南汉族人群中的分布状况。
Objective To obtain the distribution of genetic polymorphism of X chromosome specific short tandem repeat loci DXS16 in Han groups of Henan province.
目的采用短串联重复序列（STR）多态位点的复合扩增方法，研究孕妇血浆中胎儿DNA基因型。
Objective To study the fetal DNA in maternal plasma using multiplex PCR amplification of the short tandem repent (STR) systems.
利用紫外光谱结合支持向量机(SVM)模式识别原理建立了短串联重复序列(STR)的分型方法。
An approach for genotyping of STR locus based on ultraviolet (UV) spectroscopy and support vector machine (SVM) was studied.
术后2、4、6、8和12周后各组取出，观察形态学、组织学和免疫组织化学变化，并行短串联重复位点检测。
The morphological, histological, ultrastructure, and immunohistochemistry examinations were made and short tandem repeat loci were detected 2, 4, 6, 8, and 12 weeks later.
由于人类基因组包含有许多串联重复的短序列基因，它们具有很大的个体差异。
The human genome contains many loci where short base sequences are repeated in tandem, with great variation between individuals in the number of such repeats.
由于人类基因组包含有许多串联重复的短序列基因，它们具有很大的个体差异。
The human genome contains many loci where short base sequences are repeated in tandem, with great variation between individuals in the number of such repeats.
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