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

Single-cell chromosomal imbalances detection by array CGH

12 May 2006

Abstract excerpt

Genomic imbalances are a major cause of constitutional and acquired disorders. Therefore, aneuploidy screening has become the cornerstone of preimplantation, prenatal and postnatal genetic diagnosis, as well as a routine aspect of the diagnostic workup of many acquired disorders. Recently, array comparative genomic hybridization (array CGH) has been introduced as a rapid and high-resolution method for the...

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 About Contact Helena Bioinformatics

Source

Identifiers

PMID: 16698960
DOI: 10.1093/nar/gkl336

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Single-cell chromosomal imbalances detection by array CGHPMID 16698960Read ↗

New array approaches to explore single cells genomesSemantic proximity Read ↗

Aneuploidy detection in single cells using DNA array-based comparative genomic hybridizationSemantic proximity Read ↗

Single cell CGH analysis reveals a high degree of mosaicism in human embryos from patients with balanced structural chromosome aberrationsSemantic proximity Read ↗

Comprehensive chromosomal analysis of human preimplantation embryos using whole genome amplification and single cell comparative genomic hybridizationSemantic proximity Read ↗

PGD for a complex chromosomal rearrangement by array comparative genomic hybridizationSemantic proximity Read ↗

Chromosome instability is common in human cleavage-stage embryos.Semantic proximity Read ↗

Whole genome scanning as a cytogenetic tool in hematologic malignanciesSemantic proximity Read ↗

Human molecular cytogenetics: from cells to nucleotidesSemantic proximity Read ↗

Detailed chromosomal and molecular genetic analysis of single cells by whole genome amplification and comparative genomic hybridisationSemantic proximity Read ↗

Detection of ≥1 Mb microdeletions and microduplications in a single cell using custom oligonucleotide arraysSemantic proximity Read ↗

High resolution array-CGH analysis of single cellsSemantic proximity Read ↗

Prenatal detection of unbalanced chromosomal rearrangements by array CGHSemantic proximity Read ↗

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