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  • 1
    Digitale Medien
    Digitale Medien
    Springer
    International journal of legal medicine 110 (1997), S. 177-180 
    ISSN: 1437-1596
    Schlagwort(e): Key words DNA polymorphism ; Short tandem repeats (STRs) ; Paternity testing
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin , Rechtswissenschaft
    Notizen: Abstract In order to apply a set of nine STR loci in parentage testing, we performed a population genetic study on a sample of the Flemish population. Genotypes for HUMHPRTB, HUMFABP, HUMCD4, HUMCSF1PO, HUMTH01, HUMPLA2A, HUMPLA2A1, HUMF13A01, HUMCYAR04 and HUMLIPOL were determined using three triplex PCR reactions and silver staining. Allele frequencies showed no deviation from Hardy-Weinberg equilibrium. The frequency distribution agreed well with other Caucasian populations but three intermediate fragments, not previously found in Caucasians, were observed. We then resolved a series of 151 parentage disputes of which 103 were exclusions. In six cases, evidence for exclusion was obtained by only one informative STR locus out of eight for male children or out of nine for female children. These exclusions were confirmed with additional polymorphic markers. In one case of inclusion, a paternal allele expanded with one repeat unit of HUMHPRTB. This observation illustrates that STRs do not differ from other genetic systems in the fact that more than one excluding locus is required before exclusion is demonstrated.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    ISSN: 1437-1596
    Schlagwort(e): Key words Short tandem repeat (STR) ; Mutation ; DNA analysis ; Alleles ; Paternity testing
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin , Rechtswissenschaft
    Notizen: Abstract During routine paternity testing a mutation of a paternal allele at the HPRTB locus was observed. The opportunity was taken to analyse this mutation at a molecular level. The repeat sequence is flanked by an imperfect repeat sequence and this region could be involved in the mutation mechanism. For this reason, we also examined the structure of “intermediate” alleles. Sequencing confirmed the insertion of a perfect repeat motif and revealed a deletion of a dinucleotide some 50 nucleotides downstream from the repeat sequence for the intermediate alleles. It is likely that these intermediate alleles are rare biallelic deletion polymorphisms and are probably not involved in the mutation or variation mechanism of this locus.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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