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Article

Prospective first-trimester screening for trisomy 21 in 30,564 pregnancies

1 Jun 2005

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Share to Assisted Reproductive Technology and Twin Pregnancy
Share to Gestational Trophoblastic Disease Studies
Share to Prenatal Screening and Diagnostics

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 15970804
DOI: 10.1016/j.ajog.2005.03.021

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Prospective first-trimester screening for trisomy 21 in 30,564 pregnanciesPMID 15970804Read ↗

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Cell-free DNA screening for trisomy 21 in twin pregnancy: a large multicenter cohort studySemantic proximity Read ↗

Retrospective details of false-positive and false-negative results in non-invasive prenatal testing for fetal trisomies 21, 18 and 13Semantic proximity Read ↗

Adjusting the risk for trisomy 21 on the basis of second-trimester ultrasonographySemantic proximity Read ↗

What is the true fetal loss rate in pregnancies affected by trisomy 21 and how does this influence whether first trimester detection rates are superior to those in the second trimester?Semantic proximity Read ↗

Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18Semantic proximity Read ↗

Evidence-based obstetric ethics and informed decision-making by pregnant women about invasive diagnosis after first-trimester assessment of risk for trisomy 21Semantic proximity Read ↗

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

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

First‐trimester screening for trisomy 21 in Denmark: implications for detection and birth rates of trisomy 18 and trisomy 13Semantic proximity Read ↗

European Non‐Invasive Trisomy Evaluation (EU‐NITE) study: a multicenter prospective cohort study for non‐invasive fetal trisomy 21 testingSemantic proximity Read ↗

Screening for trisomies 21, 18 and 13 by cell‐free <scp>DNA</scp> analysis of maternal blood at 10–11 weeks' gestation and the combined test at 11–13 weeksSemantic proximity Read ↗

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