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

Maternal prenatal screening programs that predict trisomy 21, trisomy 18, and neural tube defects in offspring

21 Feb 2023

Abstract excerpt

OBJECTIVE: To determine the efficacy of three different maternal screening programs (first-trimester screening [FTS], individual second-trimester screening [ISTS], and first- and second-trimester combined screening [FSTCS]) in predicting offspring with trisomy 21, trisomy 18, and neural tube defects (NTDs). METHODS: A retrospective cohort involving 108,118 pregnant women who received prenatal screening tests...

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 Folate and B Vitamins Research
Share to Prenatal Screening and Diagnostics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 36809370
DOI: 10.1371/journal.pone.0281201

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Maternal prenatal screening programs that predict trisomy 21, trisomy 18, and neural tube defects in offspringPMID 36809370Read ↗

Performance analysis of non-invasive prenatal testing for trisomy 13, 18, and 21: A large-scale retrospective study (2018–2021)Semantic proximity Read ↗

Accuracy of first‐trimester combined test in screening for trisomies 21, 18 and 13Semantic proximity Read ↗

Evaluation of the Z‐score accuracy of noninvasive prenatal testing for fetal trisomies 13, 18 and 21 at a single centerSemantic proximity Read ↗

Clinical performance of non‐invasive prenatal testing for trisomies 21, 18 and 13 in twin pregnancies: A cohort study and a systematic meta‐analysisSemantic 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 ↗

Non-invasive prenatal testing for the detection of trisomy 13, 18, and 21 and sex chromosome aneuploidies in 68,763 casesSemantic proximity Read ↗

A Retrospective Single-center Analysis of Prenatal Diagnosis and Follow-up of 626 Chinese Patients with Positive Non-invasive Prenatal Testing ResultsSemantic proximity Read ↗

Prenatal screening for trisomy 21: recent advances and guidelinesSemantic proximity Read ↗

Retrospective analysis of non-invasive prenatal testing results in 8237 pregnant women in Luohe DistrictSemantic proximity Read ↗

Combined fetal fraction to analyze the Z-score accuracy of noninvasive prenatal testing for fetal trisomies 13, 18, and 21Semantic proximity Read ↗

Prenatal diagnostic testing and atypical chromosome abnormalities following combined first‐trimester screening: implications for contingent models of non‐invasive prenatal testingSemantic proximity Read ↗

A Critical Evaluation of Validation and Clinical Experience Studies in Non-Invasive Prenatal Testing for Trisomies 21, 18, and 13 and Monosomy XSemantic proximity Read ↗

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