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Article

Identification of dual false indirect exclusions on the D5S818 and FGA loci.

Legal medicine (Tokyo, Japan) - 1 Jan 2011

Jiang Wenxiao, Kline Margaret, Hu Peter, Wang Yue

Abstract excerpt

Here, we present a case in which the result of a maternity test was obscured due to two false indirect exclusions that occurred in two out of 15 genetic loci through the use of the AmpFlSTR Identifiler PCR Amplification kit (Applied Biosystems, Foster City, CA). The Identifiler kit failed to ampl...

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Source

Identifiers

PMID: 21030286
DOI: 10.1016/j.legalmed.2010.08.006

Genes

FGA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-21030286-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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Research trail→

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Identification of dual false indirect exclusions on the D5S818 and FGA loci.PMID 21030286Read ↗

A silent allele in the locus D19S433 contained within the AmpFlSTR Identifiler PCR Amplification Kit.Semantic proximity Read ↗

A single mutation in the FGA locus responsible for false homozygosities and discrepancies between commercial kits in an unusual paternity test case.Semantic proximity Read ↗

Unusual association of three rare alleles and a mismatch in a case of paternity testing.Semantic proximity Read ↗

D5S818 Typing Discrepancy Between PowerPlex(®) Fusion and Other STR Kits Including GlobalFiler(®) Caused by a One-base Deletion in 31 Nucleotides Upstream of the Repeat Region.Semantic proximity Read ↗

Identification of a discordant genotype at the D2S1338 locus between Identifiler Plus®16 kit and Power Plex®21 system kit.Semantic proximity Read ↗

Risk analysis of duo parentage testing with limited STR loci.Semantic proximity Read ↗

A silent allele in the locus D5S818 contained within the PowerPlex®21 PCR Amplification Kit.Semantic proximity Read ↗

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Microsatellite mutation in the maternally/paternally transmitted D18S51 locus: two cases of allele mismatch in the child.Semantic proximity Read ↗

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