We can't accept duplications or digital printouts.
我们不能接受的重复或数码打印输出。
Aim: To improve and regulate cellular immune functions, and inhibit viral duplications.
目的：提高和调节细胞免疫功能及病毒复制抑制功能。
These deletions or duplications, also called copy-number changes, can change the dosage of a gene.
这些缺失或者是重复，也被称做是拷贝数的改变，能改变一个基因的数目。
In many cases, duplications and deletions have no effect, but occasionally they can lead to disease.
大多数情况下，基因的重复和缺失并不会对人体造成任何影响，但某些情况下它们会导致疾病。
Phylogenetic analysis suggests the amphioxus actin genes have clearly undergone extensive expansion through tandem duplications.
进化分析的结果显示，文昌鱼的肌动蛋白基因家族可能通过串联重复而发生了扩增。
We identified several types of cyclin genes in the rice genome and characterized them by phylogenetic, tandem and segmental duplications analyses.
我们确定了几个类型在水稻基因组的细胞周期蛋白基因和特征的系统发育，串联重复片段的分析。
This same study found that other genes involved in connectivity between neurons - such as neurexin - were also affected by duplications or deletions.
同一项研究发现，涉及神经元之间连通性的其它一些基因(如neurexin)也受到复制和删除的影响。
Their study looked for chromosomal deletions and duplications known as copy number variants (CNV) and found that these were present in 16% of the children with ADHD.
他们研究被称为拷贝数变异（CNV）的染色体的删减和复制，发现在患有多动症的儿童中有 16%都存在。
If it is truly difficult to present the original document or physical evidence, then duplications, photographs, copies, or extracts of the original evidence may be admitted.
提交原件或者原物确有困难的，可以提交复制品、照片、副本、节录本。
Looking at the human genome as a "book of life" they have mapped vast Numbers of variations in letters or short words - but missed much larger deletions and duplications of pages or chapters.
如果把人类基因组视作“生命之书”，他们绘制了大量字母或短语的变异——但忽视了“书”中篇幅更大的整页乃至整章的删节和重复内容。
Comparative analysis and evolutionary analysis of the clustered genes and other peroxidase family members revealed that the gene cluster occurred by tandemly gene duplications(from osp5 to osp1 );
对5个基因间的两两比较分析和进化分析结果表明：该基因簇是通过一系列的串联基因复制事件而形成；
Methods Duplications or deletions of?PMP22gene were detected in 113 CMT cases, 4 HNPP cases and 50 normal controls by using real-time quantitative PCR. Results (Thirty-six) of 113 CMT cases had the?
方法采用实时荧光定量PCR检测113个腓骨肌萎缩症家系先证者、4个遗传性压力易感性神经病家系先证者和50名正常人PMP22基因重复或缺失突变。
Methods Duplications or deletions of?PMP22gene were detected in 113 CMT cases, 4 HNPP cases and 50 normal controls by using real-time quantitative PCR. Results (Thirty-six) of 113 CMT cases had the?
方法采用实时荧光定量PCR检测113个腓骨肌萎缩症家系先证者、4个遗传性压力易感性神经病家系先证者和50名正常人PMP22基因重复或缺失突变。
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