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

Detection of genetic abnormalities by using CVS and FISH prior to fetal reduction in sonographically normal appearing fetuses

12 Aug 2013

Abstract excerpt

OBJECTIVE: To examine the ability of chorionic villus sampling (CVS) and fluorescence in situ hybridization (FISH) to detect aneuploidy before first trimester fetal reduction (FR) in sonographically normal-appearing fetuses. METHODS: A retrospective review of 470 patients referred to our unit for FR from January 2007-March 2011. Prenatal diagnosis was offered to all. FR was performed after next-day FISH results....

Read the complete abstract on PubMed

Topics

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

Share to Assisted Reproductive Technology and Twin Pregnancy
Share to Fetal and Pediatric Neurological Disorders
Share to Prenatal Screening and Diagnostics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 23939830
DOI: 10.1002/pd.4213

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Detection of genetic abnormalities by using CVS and FISH prior to fetal reduction in sonographically normal appearing fetusesPMID 23939830Read ↗

First trimester diagnosis and screening for fetal aneuploidySemantic proximity Read ↗

Prenatal diagnosis of chromosomal mosaicism in over 1600 cases using array comparative genomic hybridization as a first line testSemantic proximity Read ↗

National decline in invasive prenatal diagnostic procedures in association with uptake of combined first trimester and cell‐free DNA aneuploidy screeningSemantic proximity Read ↗

Chorionic villus sampling (CVS) and fluorescence <i>in situ</i> hybridization (FISH) for a rapid first‐trimester prenatal diagnosisSemantic proximity Read ↗

Diagnostic testing after positive results on cell free DNA screening: CVS or Amnio?Semantic proximity Read ↗

What is the role of the 11- to 14-week ultrasound in women with negative cell-free DNA screening for aneuploidy?Semantic proximity Read ↗

Chromosomal microarray in fetuses with increased nuchal translucencySemantic proximity Read ↗

Prenatal diagnosis using combined quantitative fluorescent polymerase chain reaction and array comparative genomic hybridization analysis as a first‐line test: results from over 1000 consecutive casesSemantic proximity Read ↗

Identification of submicroscopic chromosomal aberrations in fetuses with increased nuchal translucency and apparently normal karyotypeSemantic proximity Read ↗

Fetal nuchal translucency scan and early prenatal diagnosis of chromosomal abnormalities by rapid aneuploidy screening: observational studySemantic proximity Read ↗

(Potential) false-negative diagnoses in chorionic villi and a review of the literatureSemantic proximity Read ↗

Cytogenetic study of spontaneous abortions using semi‐direct analysis of chorionic villi samples detects the broadest spectrum of chromosome abnormalitiesSemantic proximity Read ↗

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