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30个InDel在河南汉族人群中的法医学应用 被引量:4

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摘要 插入/缺失(insertion/deletion,InDel)多态性是指基因组中插入或缺失不同大小的 DNA 片段所形成的多态性遗传标记[1]。InDel 为一种特殊类型的二等位基因遗传标记,PCR 产物能通过现有的毛细管电泳平台进行分型检测,容易获得较短的扩增片段,尤其适合高度降解的生物样本分型,突变率低,适合亲缘关系鉴定。
出处 《法医学杂志》 CAS CSCD 2015年第1期61-63,共3页 Journal of Forensic Medicine
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参考文献6

  • 1Weber JL, David D, Heil J, et ol. Human diallelic insertion/deletion polymorphisms[J]. Am J Hum Genet, 2002,71 (4) :854-862.
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二级参考文献16

  • 1李莉,李荣宇,李成涛,柳燕,林源,阙庭志,孙美倩,李瑶.31个SNP位点多重PCR扩增和芯片分型技术的建立及其法医学应用[J].法医学杂志,2005,21(2):90-95. 被引量:10
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