By detecting its structure in the tumour tissue, we find that the sum of its deletion or mutation rate reaches 35%.
通过检测肿瘤组织中该基因的结构，发现该基因在肿瘤组织中的缺失或突变率的总和达到35%。
Most of the chlorophyll deletion occurred in M1 were belonged to somatic mutation or caused by radiation injury so that they usually were not inheritable.
在M_1所产生的叶绿素缺失中，大多数属于体细胞突变，或是由于辐射损伤所致，一般是不能遗传的；
This can occur through a mutation in the gene's DNA sequence or through deletion of the gene.
这种缺失可能起源于基因的突变或者通过基因序列的缺失而产生。
DNA damage caused by many factors may lead to missense mutation, deletion or illegal recombination.
多种因素可以引起DNA损伤而最终导致基因产生错义突变、缺失或错误重组。
FAP is a monogenetic disease and is caused by the mutation or deletion of the adenomatous polyposis coli (APC) gene which is found on chromosome 5.
FAP是一种单基因遗传病，是由APC基因的突变或缺失引起的(apc)基因是5号染色体上发现的。
FAP is a monogenetic disease and is caused by the mutation or deletion of the adenomatous polyposis coli (APC) gene which is found on chromosome 5.
FAP是一种单基因遗传病，是由APC基因的突变或缺失引起的(apc)基因是5号染色体上发现的。
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