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

An update on chromosome deletion and microdeletion syndromes.

Current opinion in pediatrics - 1 Dec 1998

Shapira S K

Abstract excerpt

Chromosome deletion and microdeletion syndromes account for an increasing number of clinically recognizable genetic conditions. New deletion syndromes continue to be characterized, and a number of previously described syndromes are being found to be due to chromosomal deletions or microdeletions. Fluorescent in situ hybridization technologies are in wide clinical use to diagnose deletion and microdeletion...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Aberrations
Share to Chromosome Deletion
Share to Chromosome Mapping

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

Share to Genetic Testing

Share to In Situ Hybridization, Fluorescence

Share to Molecular Biology

Share to Phenotype

Share to Prognosis

Source

Identifiers

PMID: 9848023
DOI: 10.1097/00008480-199810060-00015

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

An update on chromosome deletion and microdeletion syndromes.PMID 9848023Read ↗

The genetics of microdeletion and microduplication syndromes: an update.Semantic proximity Read ↗

Microdeletion and microduplication syndromes.Semantic proximity Read ↗

Microdeletion and Microduplication SyndromesSemantic proximity Read ↗

Microdeletion syndromes.Semantic proximity Read ↗

Human molecular cytogenetics: from cells to nucleotidesSemantic proximity Read ↗

Common recurrent microduplication syndromes: Diagnosis and management in clinical practiceSemantic proximity Read ↗

Novel microdeletion syndromes.Semantic proximity Read ↗

What have studies of genomic disorders taught us about our genome?Semantic proximity Read ↗

Phenotypes of 8q13.2-q13.3 microdeletion: Case report and literature review of an emerging recurrent microdeletion syndrome.Semantic proximity Read ↗

Chromosomal microdeletions and genes' functions: a cluster of chromosomal microdeletions and the deleted genes' functions.Semantic proximity Read ↗

Expanding Genotype/Phenotype Correlation in 2p11.2-p12 Microdeletion Syndrome.Semantic proximity Read ↗

Review of the Pathophysiology and Clinical Manifestations of 22q11.2 Deletion and Duplication SyndromesSemantic proximity Read ↗

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