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

Use of X-linked short tandem repeat loci in routine parentage casework.

Transfusion - 1 Jun 2007

Silveira Debora, Silva Fabiana F, Jesus Priscila R, Whittle Martin R

Abstract excerpt

BACKGROUND: Dealing with genetic inconsistencies in parentage testing, especially in motherless cases, remains a continual difficulty. STUDY DESIGN AND METHODS: Four difficult cases, comprising two trios and two duos, were selected from routine parentage testing casework. In these, relatively low...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomes, Human, X
Share to Fathers
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Parents

Share to Quantitative Trait Loci

Share to Tandem Repeat Sequences

Source

Identifiers

PMID: 17524096
DOI: 10.1111/j.1537-2995.2007.01238.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17524096-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

Use of X-linked short tandem repeat loci in routine parentage casework.PMID 17524096Read ↗

Forensic usefulness of a 25 X-chromosome single-nucleotide polymorphism marker set.Semantic proximity Read ↗

Comparative evaluation of alternative batteries of genetic markers to complement autosomal STRs in kinship investigations: autosomal indels vs. X-chromosome STRs.Semantic proximity Read ↗

Assessing paternities with inconclusive STR results: The suitability of bi-allelic markers.Semantic proximity Read ↗

The risk of false inclusion of a relative in parentage testing - an in silico population study.Semantic proximity Read ↗

Combining autosomal and Y-chromosomal short tandem repeat data in paternity testing with male child: methods and application.Semantic proximity Read ↗

Assessing false paternity risk in simulated motherless cases from more than 20 000 real exclusion trios.Semantic proximity Read ↗

Use of X-linked short tandem repeats loci to confirm mutations in parentage caseworks.Semantic proximity Read ↗

Evaluation of HLA in detection of non-parentage among known false trios.Semantic proximity Read ↗

[Examples of application of X chromosomal markers in familial investigations and personal identification].Semantic proximity Read ↗

Paternal exclusion: allele sharing in microsatellite testing.Semantic proximity Read ↗

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

Rapid and efficient resolution of parentage by amplification of short tandem repeats.Semantic proximity Read ↗

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