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 high-resolution SNP arrays in the investigation of fetuses with ultrasound malformations: 5 years of clinical experience.

Clinical genetics - 1 Sept 2014

Liao C, Fu F, Li R, Xie G-E, Zhang Y-L, Li J, Li D-Z

Abstract excerpt

Chromosome microarray analysis (CMA) has proven to be a powerful tool in postnatal patients with intellectual disabilities, and it is increasingly used in prenatal diagnosis. However, its diagnostic capabilities in prenatal diagnosis vary, and clinical experiences have failed to establish a consensus regarding CMA indications, the design and resolution of microarrays, and the notification and interpretation of...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomes, Human
Share to Congenital Abnormalities

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Copy Number Variations

Share to Genetic Variation

Share to Microarray Analysis

Share to Polymorphism, Single Nucleotide

Share to Prenatal Screening and Diagnostics

Share to Ultrasonography, Prenatal

Source

Identifiers

PMID: 24000829
DOI: 10.1111/cge.12271

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

Implementation of high-resolution SNP arrays in the investigation of fetuses with ultrasound malformations: 5 years of clinical experience.PMID 24000829Read ↗

Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis.Semantic proximity Read ↗

Prenatal Chromosomal Microarray Analysis: Does Increased Resolution Equal Increased Yield?Semantic proximity Read ↗

Diagnostic performance of chromosomal microarray and whole exome sequencing in fetal structural anomalies: a single-center retrospective studySemantic proximity Read ↗

Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalitiesSemantic proximity Read ↗

0.5 Mb array as a first-line prenatal cytogenetic test in cases without ultrasound abnormalities and its implementation in clinical practice.Semantic proximity Read ↗

Prenatal detection of copy number variants.Semantic proximity Read ↗

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

Meeting the challenge of interpreting high-resolution single nucleotide polymorphism array data in prenatal diagnosis: does increased diagnostic power outweigh the dilemma of rare variants?Semantic proximity Read ↗

The role of chromosomal microarray and exome sequencing in prenatal diagnosisSemantic proximity Read ↗

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

Prenatal chromosomal microarray testing of fetuses with ultrasound structural anomalies: A prospective cohort study of over 1000 consecutive casesSemantic proximity Read ↗

SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay.Semantic proximity Read ↗

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