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

Development of diagnostic tools for the analysis of 5p deletions using interphase FISH.

Cytogenetics and cell genetics - 1 Jan 1997

Gersh M, Grady D, Rojas K, Lovett M, Moyzis R, Overhauser J

Abstract excerpt

Cri-du-chat syndrome is associated with a deletion of the short arm of chromosome 5. Through the phenotypic and molecular analyses of individuals with a subset of the features associated with the syndrome, the genes involved in the syndrome have been mapped to two distinct critical regions. Deletion of a critical region in 5p15.2 results in the distinct facial features associated with the syndrome as well as the...

Read the complete abstract on PubMed

Topics

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

Share to Base Sequence
Share to Chromosome Deletion
Share to Chromosome Mapping

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Cricetinae

Share to DNA Primers

Share to Genetic Markers

Share to In Situ Hybridization, Fluorescence

Share to Phenotype

Source

Identifiers

PMID: 9284926
DOI: 10.1159/000134586

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

Development of diagnostic tools for the analysis of 5p deletions using interphase FISH.PMID 9284926Read ↗

Molecular and phenotypic mapping of the short arm of chromosome 5: sublocalization of the critical region for the cri-du-chat syndrome.Semantic proximity Read ↗

Molecular definition of deletions of different segments of distal 5p that result in distinct phenotypic features.Semantic proximity Read ↗

Characterization of a complex chromosomal rearrangement in a patient with a typical catlike cry and no other clinical findings of cri-du-chat syndrome.Semantic proximity Read ↗

A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3-25 detected using whole genomic array CGH.Semantic proximity Read ↗

Multigenerational autosomal dominant inheritance of 5p chromosomal deletions.Semantic proximity Read ↗

Cri du Chat syndrome.Semantic proximity Read ↗

Variability in a family with an insertion involving 5p.Semantic proximity Read ↗

Delineation of the dup5q phenotype by molecular cytogenetic analysis in a patient with dup5q/del 5p (cri du chat).Semantic proximity Read ↗

Characterization of a de novo complex chromosomal rearrangement in a patient with cri-du-chat and trisomy 5p syndromes.Semantic proximity Read ↗

Determination of the 'critical region' for cat-like cry of Cri-du-chat syndrome and analysis of candidate genes by quantitative PCR.Semantic proximity Read ↗

Inverted duplication with terminal deletion of 5p and no cat-like cry.Semantic proximity Read ↗

Cri du chat mosaicism: an unusual case of partial deletion and partial deletion/ duplication of the short arm of chromosome 5, leading to an unusual cri du chat phenotype.Semantic proximity Read ↗

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