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Article

Multistep microsatellite mutation leading to father-child mismatch of FGA locus in a case of non-exclusion parentage.

Legal medicine (Tokyo, Japan) - 1 Sept 2015

Jia Yun Shu, Zhang Lei, Qi Li Yuan, Mei Kun, Zhou Feng Lei, Huang Dai Xin, Yi Shao Hua

Abstract excerpt

A non-exclusion paternity case with a mismatch in the autosomal short tandem repeats (STR) locus FGA is reported. The genotypes of the suspected father, the mother and the questioned child in FGA locus were 18/25, 20/26 and 20/22, respectively. Examination of 38 autosomal STR loci revealed no mismatches, and the paternity index is up to 1.3618×10(6). The haplotype of 16 Y chromosomal STR in the child matched...

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Source

Identifiers

PMID: 25979606
DOI: 10.1016/j.legalmed.2015.05.001

Genes

FGA

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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