由共同多态现象确定的线粒体单倍群与疾病的危险因素和生存率相关。
Mitochondrial haplogroups defined by common polymorphisms have been associated with risk of disease and longevity.
人类基因组遗传多态现象研究的深入，导致了法科学领域个体识别和亲权鉴定发生根本性变化。
With the study advances on DNA polymorphism of human genome, radical changes have been taking place in forensic individual identification and paternity tests.
亚甲基四氢叶酸还原酶基因突变导致的遗传多态现象可增加神经管缺陷(ntd)发生的危险性。
The genetic polymorphisms due to mutations in the methylene tetrahydrofolate reductase gene may increase the risk for NTDs.
方法应用多聚酶链反应技术及限制性片段长度多态现象对46例食管癌APC和MCC基因的LOH进行了分析。
Methods LOH at APC and MCC genetic loci in 46 specimens resected from esophageal neoplasm was studied with polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP).
以上三种基因均存在显著影响产物表达水平的多态现象，从而推测这些重要的多态改变能够影响中国人COPD的遗传易感性。
There are germline polymorphisms lying in all of the three genes that can cause significant decrease of enzymes expression and might have solid impact on genetic susceptibility of COPD.
采用抗EGFR单克隆抗体治疗后可能伴发或无严重低镁血症，针对患者EGFR多态现象进行广泛研究或许能阐明这种毒副作用的发生机理。
Comprehensive studies of EGFR polymorphisms in patients with and without severe hypomagnesaemia after treatment with anti-EGFR monoclonal antibodies might shed further light on this toxicity.
采用抗EGFR单克隆抗体治疗后可能伴发或无严重低镁血症，针对患者EGFR多态现象进行广泛研究或许能阐明这种毒副作用的发生机理。
Comprehensive studies of EGFR polymorphisms in patients with and without severe hypomagnesaemia after treatment with anti-EGFR monoclonal antibodies might shed further light on this toxicity.
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