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Transfusion ; 61(3): 678-681, 2021 03.
Artigo em Inglês | MEDLINE | ID: mdl-33084042

RESUMO

BACKGROUND: When the mother's DNA profile is not available for paternity testing, there is a smaller probability that a locus will exclude an alleged father. This study aims to evaluate the risk of potential false paternity inclusions in motherless cases. STUDY DESIGN AND METHODS: More than 20 000 duos were generated by removing the maternal genotypes from exclusion trios. After recalculating paternity in these duos, any found inclusions would be false. RESULTS: The use of an appropriate number of loci, mutation model, and mutation rates to analyze motherless paternity cases was robust against false inclusions. A single potential false inclusion was observed in a case wherein kinship plays a role. This result highlights the importance of testing the mother when available and of obtaining information on family circumstances for the proper handling of cases involving related individuals. CONCLUSION: The guidelines we used here were sufficient to avoid false inclusions in a data set of more than 20 000 motherless cases.


Assuntos
Loci Gênicos , Repetições de Microssatélites , Alelos , Simulação por Computador , Feminino , Genótipo , Humanos , Masculino , Mães , Mutação , Paternidade , Probabilidade
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