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

Non-pathological complete paternal uniparental isodisomy of chromosome 2 revealed in a maternity testing case.

International journal of legal medicine - 1 Jul 2019

Chen Man, Jiang Jian, Li Chen, Ren He, Chen Wei, Liu Zhiyong, Cheng Feng, Zhao Jing, Chen Tong, Chen Chuguang, Yan Jiangwei

Abstract excerpt

We present a duo paternity test case to assess the biological relationship between a woman and her female child. After analyzing 57 autosomal and 19 X-chromosomal short tandem repeat loci, mother-daughter exclusions were discovered at four loci, which were all located on chromosome 2. Further testing of whole-genome single nucleotide polymorphisms confirmed that the daughter had complete uniparental disomy (UPD)...

Read the complete abstract on PubMed

Topics

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

Share to Child
Share to Chromosomes, Human, Pair 2

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Markers

Share to Microsatellite Repeats

Share to Paternity

Share to Polymorphism, Single Nucleotide

Share to Uniparental Disomy

Source

Identifiers

PMID: 29802460
DOI: 10.1007/s00414-018-1857-x

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

Non-pathological complete paternal uniparental isodisomy of chromosome 2 revealed in a maternity testing case.PMID 29802460Read ↗

Inference of maternal uniparental disomy of the entire chromosome 2 from a paternity test.Semantic proximity Read ↗

Genetic analysis of chromosome 2 copy-neutral loss of heterozygosity in paternity testing.Semantic proximity Read ↗

Confirmation of Paternity despite Three Genetic Incompatibilities at Chromosome 2.Semantic proximity Read ↗

Multiple methods used for type detection of uniparental disomy in paternity testing.Semantic proximity Read ↗

Effect of uniparental disomy in parentage testing.Semantic proximity Read ↗

Uniparental disomy of chromosome 21: A statistical approach and application in paternity tests.Semantic proximity Read ↗

Non-pathological paternal isodisomy of chromosome 2 detected from a genome-wide SNP scan.Semantic proximity Read ↗

Non-paternity and prenatal genetic screeningSemantic proximity Read ↗

Non-paternity and prenatal genetic screeningSemantic proximity Read ↗

Implications of uniparental disomy in forensic kinship testing: A case study of paternal isodisomy on chromosome 3.Semantic proximity Read ↗

Reinvestigations of six unusual paternity cases by typing of autosomal single-nucleotide polymorphisms.Semantic proximity Read ↗

An incest case with three biological brothers as alleged fathers: Even 22 autosomal STR loci analysis would not suffice without the mother.Semantic proximity Read ↗

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