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- The mutation of stepladder. 折梯的变种。
- Correlation Between the Mutation of the DCC Gene Codon 201 and Gastric Cancer. DCC基因201密码子突变与胃癌相关性的研究
- The mutation,G2043R is cause of patient with DEB.It is a mutation of de novo. COL7A1基因的G2043R突变可能是引起本例临床表现的原因,且是一个denovo突变。
- Our teacher has mutation of sounds suddenly. 我们的老师突然语音发生了变化。
- Objective To analyse the mutation of ADAR gene in a pedigree with dyschromatosis symmetrical hereditaria. 目的探讨遗传性对称性色素异常症(DSH)一家系ADAR基因突变情况。
- The mutation of HBV BCP has some relation with the genotypes of HBV and DNA level. HBVBCP的突变株HBV基因型及DNA含量有一定的相关性。
- Objective To analyse the mutation of pathogenic gene TSC2 in tuberous sclerosis complex (TSC). 摘要目的分析结节性硬化症(TSC)致病基因TSC2突变方式。
- Objective:To explore the mutation of receptor tyrosine kinase ( RET ) gene in sporadic medullary thyroid carcinoma. 目的:研究散发型甲状腺髓样癌酪氨酸激酶受体基因(RET)的突变情况。
- The mutation of Chinese style style maintained antediluvian Gu Yun already, added comfortable sense again. 中式风格的变异既保持了古风古韵，又增加了舒适的感觉。
- Conclusion The mutation of prothrombin G20210A is unlikely to be an independent risk factor for coronary heart d... 结论凝血酶原基因G20210A突变不是中国汉族人群冠心病的主要致病因素。
- Pseudomonas fluorescens A46 was a phage resistant strain obtained from the mutation of the strain K1005 by using U. 荧光假单胞菌A46是通过紫外线诱变K1005菌株所得到的一株抗噬菌体菌株。
- Results: The mutation of the new alleles of 2 pedigrees was increasing and decreasing a single repeat. 结果:2个家系中子代新产生的等位基因变异表现为一个重复单位的增加或减少。
- Factors arising from the mutation of the impulse from the West, but also from the tradition of its own fissile. 引起这场突变的因素有来自西方的冲激，也有来自传统自身的裂变。
- Objective To investigate the relationship between the mutation of growth hormone-related genes and primary amenorrhea. 摘要目的探讨生长激素相关基因突变与原发闭经的关系。
- Conclusion: The mutation of alleles often exists at the long, highly polymorphic tandem repeats in STRs. 结论:STR基因座的长的、多态性高的串联重复区是等位基因突变的敏感点。
- By the usual Darwinian dynamics of natural selection, the mutation of altitude acclimation comes to dominate the village gene pool. 根据达尔文自然选择动态的惯例，适应高地生活的变异人种就开始主宰村子的基因库。
- Abnormal PTEN expression is associated with PTEN gene mutation, the mutation of PTEN gene is the main mechanism of the inactivation of PTEN gene. 2. 中文摘要结论1．PTEN蛋白表达异常与PTEN基因突变有关，PTEN基因突变是基因失活的重要机制之一。
- Abstract Objective: To investigate the mutation of RET Proto-oncogene in sporadic Hirschsprung's disease (HD) in Chinese population. 摘要目的：明确中国散发先天性巨结肠症是否有原癌基因RET突变。
- Objective To investigate a possible association between the mutation of human prothrombin gene G20210A and coronary heart disease (CHD). 目的探讨凝血酶原基因G20210A突变与中国汉族人群冠心病的相关性。
- Objective: To investigate the relationship between the mutation of ABCB4 gene exon 12 and intrahepatic cholestasis of pregnancy(ICP). 目的探讨ABCB4基因外显子12的突变与妊娠期肝内胆汁淤积症(ICP)发病的关系。
