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

Nuchal translucency and the acceptance of invasive prenatal chromosomal diagnosis in women aged 35 and older

1 Jun 2001

Abstract excerpt

OBJECTIVE: To investigate the effect of nuchal translucency screening on use of prenatal diagnosis for chromosomal abnormalities in women aged 35 and older. METHODS: Two groups of women, referred to our center for prenatal karyotype diagnosis because of maternal age, were compared: one in 1995 and the other in 1999 after the introduction of nuchal translucency measurement. Each woman received nondirective genetic...

Read the complete abstract on PubMed

Topics

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

Share to Genetic Syndromes and Imprinting
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: 11384696
DOI: 10.1016/s0029-7844(01)01381-3

Provenance

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Nuchal translucency and the acceptance of invasive prenatal chromosomal diagnosis in women aged 35 and olderPMID 11384696Read ↗

Increased nuchal translucency thickness and normal karyotype: time for parental reassuranceSemantic proximity Read ↗

Fetal nuchal translucency: ultrasound screening for chromosomal defects in first trimester of pregnancy.Semantic proximity Read ↗

Detection of fetal chromosomal anomalies: does nuchal translucency measurement have added value in the era of non‐invasive prenatal testing?Semantic proximity Read ↗

Fetal nuchal translucency: ultrasound screening for fetal trisomy in the first trimester of pregnancySemantic proximity Read ↗

‘Normal’ nuchal translucency: a justification to refrain from detailed scan? Analysis of 6858 cases with special reference to ethical aspectsSemantic proximity Read ↗

Outcome of fetuses with enlarged nuchal translucency and normal karyotypeSemantic proximity Read ↗

First trimester fetal nuchal translucency: Problems with screening the general population 2.Semantic proximity Read ↗

Increased nuchal translucency in euploid fetuses—what should we be telling the parents?Semantic proximity Read ↗

Increased Nuchal Translucency as a Marker for Fetal Chromosomal DefectsSemantic proximity Read ↗

Nuchal translucency measurement in normal fetusesSemantic proximity Read ↗

A mixture model of nuchal translucency thickness in screening for chromosomal defectsSemantic proximity Read ↗

Relation between increased fetal nuchal translucency thickness and chromosomal defects.Semantic proximity Read ↗

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