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.

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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.

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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.

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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.

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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.

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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.

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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.

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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.

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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.

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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.

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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

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Easy item deletion prior to sending to kitchen.

所点菜肴在传入厨房前都可轻松取消.

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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.

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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 )

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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.

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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。

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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；

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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。

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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

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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

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