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

Sequence analysis of two de novo mutation alleles at the DXS10011 locus.

Legal medicine (Tokyo, Japan) - 1 Sept 2003

Tamura Akiyoshi, Iwata Misa, Takase Izumi, Miyazaki Tokiko, Matsui Kiyoshi, Nishio Hajime, Suzuki Koichi

Abstract excerpt

We have detected two unusual alleles at the DXS10011 locus in two paternity trio cases. In one case, one allele of the daughter was found not to have been derived from the mother but the other allele was shared with the father. In the other case, the mother and the son shared no bands. Paternity...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Chromosomes, Human, X
Share to Genetic Markers

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genotype

Share to Mutation

Share to Paternity

Share to Sequence Analysis, DNA

Share to Tandem Repeat Sequences

Source

Identifiers

PMID: 14568776
DOI: 10.1016/s1344-6223(03)00057-9

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-14568776-2026-09-02.1. Manifest publication-graph-cohort-2026-09-02.1.

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Sequence analysis of two de novo mutation alleles at the DXS10011 locus.PMID 14568776Read ↗

New sequence variants detected at DXS10148, DXS10074 and DXS10134 loci.Semantic proximity Read ↗

Sequence variation and allele nomenclature for the X-linked STRs DXS9895, DXS8378, DXS7132, DXS6800, DXS7133, GATA172D05, DXS7423 and DXS8377.Semantic proximity Read ↗

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

Paternal and maternal mutations in X-STRs: A GHEP-ISFG collaborative study.Semantic proximity Read ↗

Trinucleotide repeat polymorphism at DXS101.Semantic proximity Read ↗

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

Brother-sister incest paternity case with the same tri-allelic pattern of parents at D3S1358 locus: a tetra-allelic baby?Semantic proximity Read ↗

Identification and characterization of variant alleles at CODIS STR loci.Semantic proximity Read ↗

Characterisation of the STR markers DXS10146, DXS10134 and DXS10147 located within a 79.1 kb region at Xq28.Semantic proximity Read ↗

Validation of the X-chromosomal STR DXS6809.Semantic proximity Read ↗

DXS10011: a hypervariable tetranucleotide STR polymorphism on the X chromosome.Semantic proximity Read ↗

Characterization of mutations and sequence variants in the D21S11 locus by next generation sequencing.Semantic proximity Read ↗

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