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

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

Zhonghua fu chan ke za zhi - 25 Jul 2018

Guo Y L, Wang L, Xue S W, Qu S Z, Yang J, Xu H, Bai Z X, Liu N, Kong X D

Abstract excerpt

Objective: To investigate the value of single nucleotide polymorphism array (SNP-array) for fetuses with abnormal ultrasound findings. Method: A total of 904 fetuses with abnormal ultrasound findings were enrolled in this study from May 2015 to November 2017, and 434 (48.0%) cases received conventional karyotyping analysis at the same time. According to different abnormal ultrasound category, 904 cases were...

Read the complete abstract on PubMed

Topics

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

Share to Aneuploidy
Share to Chromosome Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Congenital Abnormalities

Share to Genetic Counseling

Share to Maternal Age

Share to Prenatal Diagnosis

Share to Ultrasonography, Prenatal

Source

Identifiers

PMID: 30078256
DOI: 10.3760/cma.j.issn.0529-567x.2018.07.005

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

[Application of single nucleotide polymorphism array in prenatal diagnosis for fetuses with abnormal ultrasound findings].PMID 30078256Read ↗

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

[Comparative study of prenatal diagnosis with single nucleotide polymorphism array and karyotype analysis].Semantic proximity Read ↗

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

Single nucleotide polymorphism array versus karyotype for prenatal diagnosis in fetuses with abnormal ultrasound: A systematic review and meta-analysis.Semantic proximity Read ↗

[Analysis of genome-wide copy number variations among fetuses with abnormalities detected by prenatal ultrasouography].Semantic proximity Read ↗

Fetal genetic findings for fetal growth restriction without structural malformations at a territory referral center: 10-year experienceSemantic proximity Read ↗

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

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

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

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

[Detection of fetal cardiac dysgenesis by SNP array technology and the variation hotspots of the local population].Semantic proximity Read ↗

The Genetic Etiology Diagnosis of Fetal Growth Restriction Using Single-Nucleotide Polymorphism-Based Chromosomal Microarray AnalysisSemantic proximity Read ↗

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