Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Long D13S317 variant allele: a cautionary case report.

Forensic science international. Genetics - 1 Jan 2015

Hedman Minttu, Palo Jukka U

Abstract excerpt

Exclusion at locus D13S317 between a father and child was observed in a kinship case, which at first glance appeared as a silent allele. However, a closer inspection using three commercial kits showed that the observed pattern is due to a long variant allele overlapping with different loci in different kits. Sequencing of the variant revealed a duplication within D13S317, that had also created an additional...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Alleles
Share to Base Sequence
Share to Molecular Sequence Data

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 25280379
DOI: 10.1016/j.fsigen.2014.08.016

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Long D13S317 variant allele: a cautionary case report.PMID 25280379Read ↗

[Analysis of genetic polymorphisms and a novel tri-allelic cloning sequence for the D13S317 locus among an ethnic Han Chinese population].Semantic proximity Read ↗

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

Large fragment Sanger sequencing identifies the newly encountered variant that caused null alleles in parentage testing.Semantic proximity Read ↗

Unusual variant alleles in commonly used short tandem repeat loci.Semantic proximity Read ↗

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

A case of tri-allelic pattern at locus D3S1358 on chromosome 3p21 inherited from paternal grandmother.Semantic proximity Read ↗

Multistep microsatellite mutation in the maternally transmitted locus D13S317: a case of maternal allele mismatch in the child.Semantic proximity Read ↗

A case of "false tri-allelic pattern" on D7S820, caused by invasion of a short SE33 allele into the bins of D7S820.Semantic proximity Read ↗

Two rare novel polymorphisms in the D8S1179 and D13S317 markers and method to mitigate their impact on human identification.Semantic proximity Read ↗

Identification of a rare off-ladder allele of the D13S325 locus during paternity testing.Semantic proximity Read ↗

An unbalanced tri-allelic pattern at the D10S1248 locus: Characteristics, genetic basis and transmission.Semantic proximity Read ↗

[Analysis of rare alleles of D13S325 falling in the range of adjacent locus].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.