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

Supernumerary marker chromosomes management in prenatal diagnosis

16 Oct 2008

Abstract excerpt

To assess the practical usefulness of array-comparative genomic hybridization (a-CGH) when supernumerary marker chromosomes (SMCs) are detected during prenatal diagnosis, we retrospectively studied SMC management in our laboratory before a-CGH availability. In this 11-year study, SMCs were observed in 20/16,810 routine karyotypes (0.12%). Their chromosomal origin, ascertained in 13 cases, remained elusive in...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomal and Genetic Variations
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: 18925665
DOI: 10.1002/ajmg.a.32532

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 23 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Supernumerary marker chromosomes management in prenatal diagnosisPMID 18925665Read ↗

Handling small supernumerary marker chromosomes in prenatal diagnosticsSemantic proximity Read ↗

Characterisation of supernumerary chromosomal markers: a study of 13 cases.Semantic proximity Read ↗

Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studiesSemantic proximity Read ↗

[Prenatal diagnosis of three fetuses with small supernumerary marker chromosomes].Semantic proximity Read ↗

Prenatal diagnosis of minute supernumerary marker chromosomes.Semantic proximity Read ↗

Retrospectively investigating the 12-year experience of prenatal diagnosis of small supernumerary marker chromosomes through array comparative genomic hybridizationSemantic proximity Read ↗

Marker chromosomes.Semantic proximity Read ↗

Prenatal diagnosis and molecular cytogenetic identification of small supernumerary marker chromosomes: analysis of three prenatal cases using chromosome microarray analysis.Semantic proximity Read ↗

Molecular characterization of 39 de novo sSMC: contribution to prognosis and genetic counselling, a prospective study.Semantic proximity Read ↗

Molecular Delineation of De Novo Small Supernumerary Marker Chromosomes in Prenatal Diagnosis, A Retrospective StudySemantic proximity Read ↗

Detection and genetic analysis of small supernumerary marker chromosomes in prenatal diagnosisSemantic proximity Read ↗

Supernumerary marker chromosomes derived from chromosome 6: Cytogenetic, molecular cytogenetic, and array CGH characterizationSemantic proximity Read ↗

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