gene deletion

Objective: The relationship between the insertion/ deletion polymorphism of angiotensin converting enzyme ( ACE) gene and the susceptibility of kidney-deficiency asthma in children was investigated.

目的探讨血管紧张素转移酶（ACE）基因插入/缺失多态性与肾虚型哮喘病易感性的关系，为今后的连锁分析打下基础。

Conclusion GSTM 1 gene deletion is not related to senile cataract formation.

结论GSTM1基因缺失与老年性白内障的发生缺乏显著关系.

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.

Objective To investigate the relationship between angiotensin converting enzyme ( ACE) gene insertion/ deletion ( I/ D) polymorphism and the severe morbidity of neonates.

目的检测血管紧张素转化酶（angiotensin converting enzyme，ACE）基因型，探讨ACE基因插入或缺失多态性与新生儿危重症的关系。

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；

The Relationship between Insertion/ Deletion Polymorphism and Serum Enzyme Levels of the Angiotensin I-converting Enzyme Gene and N-terminal Pro-B-type Natriuretic Peptide in Acute Myocardial Infarction

急性心肌梗塞患者ACE基因插入/缺失多态性与血清ACE，氨基末端脑钠尿肽相关性的研究

Objective To identify the insertion/ deletion ( I/ D) polymorphism of angiotensin converting enzyme ( ACE) gene in Chinese hypertensives complicated with brain infarction.

目的探讨血管紧张素转化酶（ACE）基因插入／缺失（I／D）多态性与中国人高血压病合并脑梗塞的关系。

Aim: To explore the polymorphism of angiotensin I converting enzyme gene insertion/ deletion in the patients with myocardial infarction ( MI).

目的：探讨心肌梗死患者（MI）血管紧张素转换酶（ACE）基因插入/缺失多态性。

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

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