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。

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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.

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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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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。

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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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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

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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。

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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。

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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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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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