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

Analysis of Xp22.31q27.1 Region Variation Detection based on SNP Array Technology.

Clinical laboratory - 1 Jan 2024

Xu Lijuan, Wang Kangying, Liu Ben

Abstract excerpt

BACKGROUND: The aim of the study was to investigate the value of single nucleotide polymorphism array (SNP array) technology in the prenatal diagnosis. METHODS: The variants in Xp22.31q27.1 region of 13 fetuses were analyzed by SNP array technology. Chromosome karyotype analysis was also performed for these fetuses and their parents. RESULTS: Chromosome karyotype analysis found no obvious chromosomal abnormality...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Aberrations
Share to Chromosome Disorders
Share to Fetus

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Karyotyping

Share to Polymorphism, Single Nucleotide

Share to Pregnancy

Share to Prenatal Diagnosis

Source

Identifiers

PMID: 38213212
DOI: 10.7754/Clin.Lab.2023.230636

Provenance

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Analysis of Xp22.31q27.1 Region Variation Detection based on SNP Array Technology.PMID 38213212Read ↗

The importance of mutation pattern in pregnancy outcomes of patients with abnormal prenatal chromosomal microarray results.Semantic proximity Read ↗

Identification of minor chromosomal defects causing abnormal foetus and spontaneous abortions.Semantic proximity Read ↗

[Application of single nucleotide polymorphism array in prenatal diagnosis for fetuses with abnormal ultrasound findings].Semantic proximity Read ↗

Clinical Utility of SNP Array Analysis in Prenatal Diagnosis: A Cohort Study of 5000 PregnanciesSemantic proximity Read ↗

[SNP-chip technology for identification of origins for prenatally detected marker chromosomes].Semantic proximity Read ↗

[Prenatal diagnosis of a fetus with Phelan-McDermid syndrome and 21q21 microdeletion by multiple genetic techniques].Semantic proximity Read ↗

[Unexpected discovery of a fetus with DMD gene deletion using single nucleotide polymorphism array].Semantic proximity Read ↗

[Application of SNP array method in prenatal diagnosis].Semantic proximity Read ↗

Does the 1.5 Mb microduplication in chromosome band Xp22.31 have a pathogenetic role? New contribution and a review of the literature.Semantic proximity Read ↗

Assessing the clinical application value of SNP-array in fetal central nervous system malformations.Semantic proximity Read ↗

Using single nucleotide polymorphism array for prenatal diagnosis in a large multicenter study in Southern China.Semantic proximity Read ↗

[Application of single nucleotide polymorphism-based array analysis for prenatal diagnosis of a fetus with de novo derivative chromosome].Semantic proximity Read ↗

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