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

Implementation of a High-Resolution Single-Nucleotide Polymorphism Array in Analyzing the Products of Conception.

Genetic testing and molecular biomarkers - 1 Jul 2016

Zhang HuiMin, Liu WeiQiang, Chen Min, Li ZhiHua, Sun XiaoFang, Wang ChenHong

Abstract excerpt

AIMS: To demonstrate the value of a whole-genome high-resolution single-nucleotide polymorphism (SNP) array for the elucidation of genetic causes underlying pregnancy loss. METHODS: The SNP array combined with SNPs and oligonucleotide probes was used to examine 60 samples of products of conception, including chorionic villi, fetal parts, and fetal blood. RESULTS: The SNP array yielded a 38.3% (23/60) abnormality...

Read the complete abstract on PubMed

Topics

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

Share to Abortion, Spontaneous
Share to Aneuploidy

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosome Aberrations

Share to DNA Copy Number Variations

Share to Fertilization

Share to Genome, Human

Share to Loss of Heterozygosity

Share to Oligonucleotide Array Sequence Analysis

Source

Identifiers

PMID: 27228077
DOI: 10.1089/gtmb.2016.0035

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

Implementation of a High-Resolution Single-Nucleotide Polymorphism Array in Analyzing the Products of Conception.PMID 27228077Read ↗

Improved assay performance of single nucleotide polymorphism array over conventional karyotyping in analyzing products of conception.Semantic proximity Read ↗

Genomic imbalance in products of conception: single-nucleotide polymorphism chromosomal microarray analysis.Semantic proximity Read ↗

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

Comprehensive genetic analysis of pregnancy loss by chromosomal microarrays: outcomes, benefits, and challenges.Semantic proximity Read ↗

Single-Nucleotide Polymorphism-Microarray Ploidy Analysis of Paraffin-Embedded Products of Conception in Recurrent Pregnancy Loss Evaluations.Semantic proximity Read ↗

Clinical utilization of chromosomal microarray analysis for the genetic analysis in subgroups of pregnancy lossSemantic proximity Read ↗

Enhanced genetic diagnosis in early pregnancy loss: an integrated approach using CNV-Seq and STR genotyping.Semantic proximity Read ↗

Whole-exome sequencing analysis on products of conception: A cohort study to evaluate clinical utility and genetic etiology for pregnancy lossSemantic proximity Read ↗

Single-nucleotide polymorphism microarray detects molar pregnancies in 3% of miscarriagesSemantic proximity Read ↗

Exploring the cause of early miscarriage with SNP-array analysis and karyotyping.Semantic proximity Read ↗

Clinical application of SNP array analysis in first-trimester pregnancy loss: a prospective study.Semantic proximity Read ↗

Identification of chromosomal abnormalities in miscarriages using single-nucleotide polymorphism arrays.Semantic proximity Read ↗

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