对单亲案的亲权鉴定，检测的多态性基因座要在8个以上。
For the purpose of identifying paternity in cases of absence of mother, more than 8 polymorphic DNA loci must be tested.
方法根据基因频率和遗传规律，推导单亲案亲权鉴定时的非父排除率。
Methods Based on the law of inheritance and allele frequency, the powers of exclusion of STR loci in motherless parentage testing (PEM) were calculated.
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.
结论本数据表明DXS10011和DXS8377在复杂的亲权鉴定中可提供高的遗传多态性信息。
Conclusion Our data indicate that DXS10011 and DXS8377 are highly informative X chromosome markers for complicated kinship analysis.
结论这16个X -STR基因座达到了法医物证学应用要求，尤其对特殊的亲权鉴定案件具有重要的应用价值。
Conclusion the 16 X-STR loci meet the application requires of forensic genetics, especially for testing the special paternity cases.
结论此10个X染色体sTR位点有较高的个体识别率，在个体识别和女孩亲权鉴定中有较高应用价值，对疾病相关研究有重要意义。
Conclusion The 10 X-chromosomal STR loci are appropriate for individual identification and paternity testing of a female child as well as for studies on related diseases.
结论此10个X染色体sTR位点有较高的个体识别率，在个体识别和女孩亲权鉴定中有较高应用价值，对疾病相关研究有重要意义。
Conclusion The 10 X-chromosomal STRs loci are appropriate for individual identification, for paternity testing involving a female child, and for studies on related disease.
结论此10个X染色体sTR位点有较高的个体识别率，在个体识别和女孩亲权鉴定中有较高应用价值，对疾病相关研究有重要意义。
Conclusion The 10 X-chromosomal STRs loci are appropriate for individual identification, for paternity testing involving a female child, and for studies on related disease.
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