deletion的例句大全

Objective To detect dystrophin gene deletion of Duchenne muscular dystrophy ( DMD ) and make DMD gene diagnosis.

目的探讨Duchenne型肌营养不良症 ( DMD ) 患者基因缺失的突变特点并进行基因诊断.

Other emendation records , e . g . addition , deletion and correction, are shown in the same way.

其他校改记录如增补 、 删节及误字改正也以同样的方式显示.

Note: Hon Albert CHAN's amendment is marked in bold and italic type or with deletion line.

注: 陈克勤议员的修正案以粗斜字体或删除线标示.

Note: Hon Albert HO's amendment is marked in bold and italic type or with deletion line.

注: 何俊仁议员的修正案以粗斜字体或删除线标示.

Note: Hon Vincent FANG's amendment is marked in bold and italic type or with deletion line.

注: 方刚议员的修正案以粗斜字体或删除线标示.

To investigate the relationship between isoniazid-resistance and Kat G gene mutation or deletion.

目的:探讨结核分枝杆菌异烟肼(inh)耐药与KatG基因突变和缺失的关系.

Graphics allow for the deletion, modification, copying, shear, translation, such as revocation of operation.

允许对图形的删除 、 修改 、 拷贝 、 剪切 、 平移 、 撤销等操作. 允许改变图元的颜色、线形、形状等.

Objective To observe the clinical effect of recessive artificial teeth repaired of first anterior molar deletion.

目的观察隐形义齿修复第1前磨牙的临床效果.

DNA damage caused by many factors may lead to missense mutation, deletion or illegal recombination.

多种因素可以引起DNA损伤而最终导致基因产生错义突变 、 缺失或错误重组.

RESULTS: All the 32 rabbits as recipients were involved in the analysis of results without deletion midway.

结果: 作为受体的32只兔全部进入结果分析,中途无脱落.

Construction of middle fragment deletion mutant with improved gene splicing by overlap extension

用改进的重叠区扩增基因拼接法构建中间缺失突变体

Easy item deletion prior to sending to kitchen.

所点菜肴在传入厨房前都可轻松取消.

The Datanodes also perform block creation, deletion, and replication upon instruction from the Namenode.

数据节点执行来自于名字节点的建立 、 删除 、 复制指令.

Replicate deletion of these records to other servers ( tombstone )

在其它服务器上复制这些记录的删除 ( 逻辑删除 )

One or more of the items could not be unmarked for deletion.

有一个或多个项目无法标记为删除.

Process instance deletion puts a heavy load on the database system.

删除过程实例会在数据库系统上产生很重的负载。

All of the patients who had parkin gene deletion mutation had tremor, rigidity and bradykinesia, but athetosis and family history of PD were not found.

所有缺失突变病例均有震颤、僵直和运动迟缓，但无异动症和PD家族史；

Results In the 6 unrelated families of PD patients, 1 case had exon 5 deletion, its hereditary manner was autosomal recessive inheritance, the patient's age at the onset was 60 years old, clinical feature was tremor, rigidity and bradykinesia, but no athetosis.

结果6例患者中，发现1例有第5外显子缺失，其遗传模式呈常染色体隐性遗传，起病年龄60岁，临床表现为震颤、僵直和运动迟缓，但无异动症。

Cloning and Expression of the Aspartase Mutant of Deletion from C-terminal End

天冬氨酸酶C端缺失突变酶基因的克隆和表达

Microcalorimetric Study on Deletion Mutagenesis of the Gene Promoter Sequences from the Extremely Halophilic Archaea

极端嗜盐古生菌启动子序列缺失突变的微量热研究