1997
DOI: 10.1002/elps.1150180930
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DNA analysis in disputed parentage: The occurrence of two apparently false exclusions of paternity, both at short tandem repeat (STR) loci, in the one child

Abstract: In cases of disputed paternity investigated by DNA analysis, it is generally accepted that at least two independent exclusions be observed before concluding that a putative father is not the biological father of the child. We report here a case in which two apparent exclusions of paternity were obtained (at the loci FESFPS and TPOX), from a total of nineteen loci examined (short tandem repeats, AMFLPs, DQA1, Polymarkers). The combined paternity index of the other seventeen loci, and of two multilocus probes (3… Show more

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Cited by 40 publications
(21 citation statements)
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“…For a conclusion of non-paternity, exclusions in more than one or two loci are practically required as the possibility of mutations or null alleles cannot be ignored (see for example Chakraborty et al 1974;Kaye 1990;Chakraborty and Stivers 1996;Gunn et al 1997;Brinkmann et al 2001). To address this, the following formulae are available.…”
Section: Resultsmentioning
confidence: 99%
“…For a conclusion of non-paternity, exclusions in more than one or two loci are practically required as the possibility of mutations or null alleles cannot be ignored (see for example Chakraborty et al 1974;Kaye 1990;Chakraborty and Stivers 1996;Gunn et al 1997;Brinkmann et al 2001). To address this, the following formulae are available.…”
Section: Resultsmentioning
confidence: 99%
“…In this procedure it was essential to have genotypes for several loci to declare non-paternity with absolute confidence with a minimum of three excluding loci to avoid false exclusions due to mutations (Gunn et al 1997). Di-nucleotide repeat microsatellites have been reported to have higher mutation rates following the step-wise mutation model (Valdes 1993) than longer repeat motifs in humans (Brinkmann et al 1999) and, more recently, in maize (Vigouroux et al 2002).…”
Section: Discussionmentioning
confidence: 99%
“…Mutations have been observed at multiple loci in the same individual for Y-STRs [22] and autosomal STRs [25] and may lead to a wrongful exclusion [26]. However, likelihood ratios that incorporate a method to take account of mutation rates across multiple loci can be used to analyse data with apparent exclusions caused by mutation events.…”
Section: Mutation Ratesmentioning
confidence: 99%