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

Clinical utility of non‐invasive prenatal testing in pregnancies with ultrasound anomalies

12 Aug 2016

Abstract excerpt

OBJECTIVE: To evaluate the application of non-invasive prenatal testing (NIPT) as an alternative to invasive diagnostic prenatal testing in pregnancies with abnormal ultrasound findings. METHODS: This was a retrospective analysis of 251 singleton and multiple pregnancies at high risk for fetal chromosomal abnormality based on findings at sonographic examination, in which NIPT was performed as a first-tier genetic...

Read the complete abstract on PubMed

Topics

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

Share to Fetal and Pediatric Neurological Disorders
Share to Genomic variations and chromosomal abnormalities
Share to Prenatal Screening and Diagnostics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 27515011
DOI: 10.1002/uog.17228

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical utility of non‐invasive prenatal testing in pregnancies with ultrasound anomaliesPMID 27515011Read ↗

Potential diagnostic consequences of applying non‐invasive prenatal testing: population‐based study from a country with existing first‐trimester screeningSemantic proximity Read ↗

Non-invasive prenatal testing: a revolutionary journey in prenatal testingSemantic proximity Read ↗

Non‐invasive prenatal testing for fetal chromosomal abnormalities by low‐coverage whole‐genome sequencing of maternal plasma <scp>DNA</scp> : review of 1982 consecutive cases in a single centerSemantic proximity Read ↗

Non-Invasive Prenatal Screening from a Genetic Counseling Prospective: Pre and Post-Genetic Counseling Regarding Rare Chromosomal Abnormalities and Incidental FindingSemantic proximity Read ↗

Social and medical need for whole genome high resolution NIPTSemantic proximity Read ↗

Recent trends in prenatal genetic screening and testingSemantic proximity Read ↗

Enlarged NT (≥3.5 mm) in the first trimester – not all chromosome aberrations can be detected by NIPTSemantic proximity Read ↗

Application of non-invasive prenatal testing for fetal chromosomal disorders in low-risk pregnancies: a follow-up study in central ChinaSemantic proximity Read ↗

The role of non-invasive prenatal testing and ultrasound in prenatal screening of fetal chromosomal abnormalities in singleton: a retrospective studySemantic proximity Read ↗

The Clinical Application of Non-invasive Prenatal Genetic Testing in the Screening of Fetal Chromosomal DiseasesSemantic proximity Read ↗

Non‐invasive prenatal testing for trisomies 21, 18 and 13: clinical experience from 146 958 pregnanciesSemantic proximity Read ↗

The influence of SNP-based chromosomal microarray and NIPT on the diagnostic yield in 10,000 fetuses with and without fetal ultrasound anomalies.Semantic proximity Read ↗

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