片语

gene deletion type缺失型基因

gene large deletion基因大片段缺失

gene rearrangement and deletion基因重排和缺失

p 16 gene homozygous deletionp基因缺失

pepB gene deletionpepB基因缺失

DAZ gene deletionDAZ基因缺失

marker gene deletion标记基因删除

p gene homozygous deletionp16基因缺失

gene homozygous deletion基因缺失

英汉例句

• The PMP22 gene deletion detected by gene diagnosis is the golden criterion for the diagnosis of HNPP.

  结论电生理检查对HNPP的诊断很重要，基因检测发现PMP22基因缺失是诊断HNPP的金标準。

• they observed no instances in the subjects with bipolar illness of the chromosome 22 gene deletion implicated in schizophrenia and the velocardiofacial syndrome.

  他们并未观察到22号染色体缺失的躁郁患者实例。这条染色体牵涉到精神分裂癥、腭心面综合征。

• Objective To investigate gene deletion and the fusion points of hybrid genes in congenital red green color vision defects.

  目的研究先天性红绿色觉异常基因缺失与杂种基因融合位点。

• In the present study, we investigated whether gene deletion of AT2 receptor causes the compensatory chaos of renin-angiotensin system in mice.

  依据上述论点，本研究利用AT2受体基因敲出小鼠，观察了AT2受体缺失后是否造成肾素-血管紧张素系统其它成分代偿性紊乱。

• Objective To investigate the relationship between the angiotensin converting enzyme (ACE) gene deletion polymorphism and cerebral infarction, hypertensive cerebral hemorrhage in Chinese.

  目的探讨血管紧张素转化酶(ace)基因缺失多态性与中国人脑梗死、高血压性脑出血的关系。

• Dual FISH technique provides specific, sensitive and direct evidence for molecular cytogenetic evaluation of gene deletion in tumors.

  双色FISH技术为评估基因的缺失提供了特异、敏感、直观的分子细胞遗传学证据。

• It is also improved M and NS genes by a site mutation and a gene deletion method.

  通过点变异和基因删除方法对M和NS基因进行改进；

• Conclusion GSTM1 gene deletion is not related to senile cataract formation.

  结论GSTM 1基因缺失与老年性白内障的发生缺乏显着关系。

• Conclusion There is no difference in frequency of CYP2A6 gene deletion between lung cancer cases and controls.

  结论CYP2A6突变基因在肺癌组及对照组中的频率分布没有差异。