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

Single nucleotide polymorphism array (SNP-array) analysis for fetuses with abnormal nasal bone.

Archives of gynecology and obstetrics - 1 Jun 2024

Xie Xiaorui, Su Linjuan, Li Ying, Shen Qingmei, Wang Meiying, Wu Xiaoqing

Abstract excerpt

PURPOSE: This study aims to evaluate the prevalence of submicroscopic chromosomal abnormalities found on single nucleotide polymorphism array (SNP array) in pregnancies with either an absent or hypoplastic nasal bone. METHODS: This retrospective study included 333 fetuses with either nasal bone hypoplasia or absence identified on prenatal ultrasound. SNP array analysis and conventional karyotyping were performed...

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

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Copy Number Variations

Share to Down Syndrome

Share to Karyotyping

Share to Maternal Age

Share to Prevalence

Share to Ultrasonography, Prenatal

Source

Identifiers

PMID: 37430178
DOI: 10.1007/s00404-023-07122-5

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

Single nucleotide polymorphism array (SNP-array) analysis for fetuses with abnormal nasal bone.PMID 37430178Read ↗

[Single nucleotide polymorphism microarray in prenatal diagnosis of fetuses with absent nasal bone].Semantic proximity Read ↗

Prenatal diagnosis and outcomes in 320 fetuses with nasal bone anomaliesSemantic proximity Read ↗

CMA-first, ES-on-demand for fetuses with absent/hypoplastic nasal bone: a real-world diagnostic pathway and outcomes in 362 fetusesSemantic proximity Read ↗

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

Relationship Between the Timing of Fetal Nasal Bone Abnormalities and Fetal Chromosomal Anomalies: A Retrospective Study in a Chinese CohortSemantic proximity Read ↗

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

Prenatal chromosomal microarray analysis in foetuses with isolated absent or hypoplastic nasal boneSemantic proximity Read ↗

Prenatal SNP array testing in 1000 fetuses with ultrasound anomalies: causative, unexpected and susceptibility CNVs.Semantic proximity Read ↗

[Prenatal genetic diagnosis of a partial 21 trisomy fetus with nasal bone dysplasia].Semantic proximity Read ↗

The Association Between Fetal Nasal Bone Hypoplasia and AneuploidySemantic proximity Read ↗

Chromosomal Microarray Analysis and Karyotype Analysis for Prenatal Diagnosis of Fetuses With Abnormal Ultrasound Soft MarkersSemantic proximity Read ↗

Identification of copy number variations among fetuses with isolated ultrasound soft markers in pregnant women not of advanced maternal ageSemantic proximity Read ↗

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