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

Array CGH analysis in high‐risk pregnancies: comparing DNA from cultured cells and cell‐free fetal DNA

24 Oct 2011

Abstract excerpt

OBJECTIVE: To compare results of array comparative genomic hybridization (CGH) on cell-free fetal (cff) DNA from amniotic fluid supernatant and DNA from cultured amniocytes in high-risk pregnancies. METHOD: We selected 48 cases of high-risk pregnancies (in utero growth retardation [IUGR] and/or at least two fetal malformations [polymalformation]). Bacterial artificial chromosome array CGH (BlueGnome) was...

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 Delete account & data About Contact Helena Bioinformatics

Source

Identifiers

PMID: 22025315
DOI: 10.1002/pd.2861

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 · 9 closest

Array CGH analysis in high‐risk pregnancies: comparing DNA from cultured cells and cell‐free fetal DNAPMID 22025315Read ↗

Copy number variation sequencing-based prenatal diagnosis using cell-free fetal DNA in amniotic fluid.Semantic proximity Read ↗

Rapid prenatal diagnosis using uncultured amniocytes and oligonucleotide array CGHSemantic proximity Read ↗

Detecting genomic imbalances in prenatal diagnosis: main hurdles and recent advancesSemantic proximity Read ↗

Microarray Analysis of Cell-Free Fetal DNA in Amniotic Fluid: a Prenatal Molecular KaryotypeSemantic proximity Read ↗

Cell-free fetal nucleic acids in amniotic fluidSemantic proximity Read ↗

Clinical application of whole-genome array CGH during prenatal diagnosis: Study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrationsSemantic proximity Read ↗

Array comparative genomic hybridization and flow cytometry analysis of spontaneous abortions and mors in utero samplesSemantic proximity Read ↗

Maternal cell contamination of prenatal samples assessed by QF-PCR genotyping.Semantic proximity Read ↗

Prenatal diagnosis of mosaic trisomy 2: Discrepancy between molecular cytogenetic analyses of uncultured amniocytes and karyotyping of cultured amniocytes in a pregnancy with severe fetal intrauterine growth restrictionSemantic proximity Read ↗

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