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亲子鉴定争议中缺陷案例的STR分型

STR typing in a deficiency case of disputed paternity.

作者信息

Fukuda M, Kishida T, Wang W, Tamaki Y

机构信息

Department of Forensic Medicine, Oita Medical University, Japan.

出版信息

Nihon Hoigaku Zasshi. 1996 Dec;50(6):422-6.

PMID:8997088
Abstract

In a case of disputed paternity where the alleged father was dead and the children and their mothers were available for testing, we analyzed 23 conventional hemogenetic markers and six short tandem repeat loci. We deduced the possible types of the alleged father and calculated the probability of paternity. Conventional phenotypings did not provide conclusive proof of paternity. In contrast, typing of the short tandem repeat loci gave a combined probability of paternity of 0.9986, establishing paternity. The present study demonstrates the power of short tandem repeat typing as a tool for solving such a deficiency case.

摘要

在一例涉及亲子关系存疑的案例中,所谓的父亲已去世,但其子女及其母亲可供检测,我们分析了23个常规血液遗传标记和6个短串联重复序列位点。我们推断出了所谓父亲的可能类型,并计算了父权概率。常规表型分析并未提供确凿的父权证据。相比之下,短串联重复序列位点的分型得出的父权联合概率为0.9986,从而确定了父权关系。本研究证明了短串联重复序列分型作为解决此类疑难案例工具的强大作用。

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