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Article

Uniparental disomy of chromosome 21: A statistical approach and application in paternity tests.

Forensic science international. Genetics - 1 Nov 2020

Cavalheiro C P, Avila E, Gastaldo A Z, Graebin P, Motta C H A, Rodenbusch R, Alho C S

Abstract excerpt

Considering the overall frequency of paternity investigation cases including mutational events, there is a real possibility that at least a fraction of all inconsistencies reported in paternity cases are caused not by polymerase slippage mutations, but to chromosomic abnormalities, as Uniparental Disomy (UPD). We report here the investigation of a trio paternity case (mother, child and alleged father), with...

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Share to Chromosomes, Human, Pair 21
Share to Electrophoresis, Capillary

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to High-Throughput Nucleotide Sequencing

Share to Models, Statistical

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Share to Sequence Analysis, DNA

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Source

Identifiers

PMID: 32911454
DOI: 10.1016/j.fsigen.2020.102368

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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