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

Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics.

1 May 1992

Abstract excerpt

We describe a method, termed reverse chromosome painting, which allows the rapid analysis of the content and breakpoints of aberrant chromosomes. The method involves the sorting of small numbers of the aberrant chromosome from short term blood culture preparations or cell lines by using bivariate flow karyotype analysis. The sorted chromosomes are amplified and biotin labelled enzymatically using a degenerate...

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: 1583656
DOI: 10.1136/jmg.29.5.299

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 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

Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics.PMID 1583656Read ↗

FISH mapping of de novo apparently balanced chromosome rearrangements identifies characteristics associated with phenotypic abnormality.Semantic proximity Read ↗

Case-specific, breakpoint-spanning DNA probes for analysis of single interphase cells.Semantic proximity Read ↗

Subtelomeric chromosome aberrations: still a lot to learn.Semantic proximity Read ↗

Carrier-specific breakpoint-spanning DNA probes: an approach to preimplantation genetic diagnosis in interphase cellsSemantic proximity Read ↗

Inversion polymorphisms and non-contiguous terminal deletions: the cause and the (unpredicted) effect of our genome architecture.Semantic proximity Read ↗

The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes.Semantic proximity Read ↗

Cytogenetic and molecular characterization of two isodicentric Y chromosomes.Semantic proximity Read ↗

Cryptic subtelomeric rearrangements and X chromosome mosaicism: a study of 565 apparently normal individuals with fluorescent in situ hybridization.Semantic proximity Read ↗

A dicentric variant of chromosome 6: characterization by use of in situ hybridisation with the biotinylated probe p308.Semantic proximity Read ↗

Rapid interphase analysis for prenatal diagnosis of translocation carriers using subtelomeric probesSemantic proximity Read ↗

FISH and cytogenetic characterization of a terminal chromosome 1q deletion: clinical case report and phenotypic implications.Semantic proximity Read ↗

De novo duplication of 12pter-->p12.1: clinical and cytogenetic diagnosis confirmed by chromosome painting.Semantic proximity Read ↗

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