1) Deletion
[英][di'li:ʃən] [美][dɪ'liʃən]
缺失变异
1.
Effects of partial deletion in the core promoter of hepatitis B virus genome on viral antigen ex-pressions;
乙型肝炎病毒核心启动子缺失变异对病毒抗原表达的影响
2) mutant strain with deletion
缺失变异株
3) insertion/deletion variation
插入/缺失变异
4) C-terminal truncated analog
C末端缺失变异体
5) deletion mutation
缺失突变
1.
Autosomal dominant congenital nuclear cataract caused by a deletion mutation in the βA1-crystallin gene;
晶体蛋白βA1基因缺失突变导致常染色体显性遗传核性先天性白内障
2.
Objective To search parkin gene deletion mutations at exons 1 to 6 in Chinese patients with praecox Parkinson s disease (PPD) and analyze them together with the clinical features of PPD.
方法 用 PPD患者外周血液提取 DNA,通过 PCR扩增、琼脂糖凝胶电泳鉴定 parkin基因外显子缺失突变 ,并结合临床资料分析。
3.
Objective To characterize the deletions of mitochondrial DNA (mtDNA) in Chinese patients with Kearns-Sayre syndrome (KSS) and chronic progressive external ophthalmolegia (CPEO) and identify deletion mutations of mtDNA be the etiology of these diseases.
在2例Kearns－Sayre综合征（KSS）和2例慢性进行性眼外肌麻痹（CPEO）患者的骨骼肌线粒体DNA（mtDNA）中发现存在单一的大片段缺失突变。
6) deletion
[英][di'li:ʃən] [美][dɪ'liʃən]
缺失突变
1.
Aim: To study the application of the mutation-sensitive molecular switch in the two deletion hotspots of EGFR gene associated with lung cancer.
目的:研究高保真DNA聚合酶介导的基因突变敏感性分子开关在肺癌EGFR基因缺失突变检测中的应用。
补充资料：21号染色体部分缺失综合征
21号染色体部分缺失综合征
病名。即21q-综合征。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条