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

High resolution genomic analysis of 18q- using oligo-microarray comparative genomic hybridization (aCGH).

American journal of medical genetics. Part A - 1 Jul 2009

Heard Patricia L, Carter Erika M, Crandall Analisa C, Sebold Courtney, Hale Daniel E, Cody Jannine D

Abstract excerpt

The advent of oligonucleotide array comparative genomic hybridization (aCGH) has revolutionized diagnosis of chromosome abnormalities in the genetics clinic. This new technology also has valuable potential as a research tool to investigate larger genomic rearrangements that are typically diagnosed via routine karyotype. aCGH was used as a tool for the high-resolution analysis of chromosome content in individuals...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 18

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

Share to Comparative Genomic Hybridization

Share to Homozygote

Share to Karyotyping

Share to Microarray Analysis

Share to Ploidies

Share to Software

Source

Open in PubMed Open full text

Identifiers

PMID: 19533772
DOI: 10.1002/ajmg.a.32900
PMCID: PMC2731576

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

High resolution genomic analysis of 18q- using oligo-microarray comparative genomic hybridization (aCGH).PMID 19533772Read ↗

Rapid array-based genomic characterization of a subtle structural abnormality: a patient with psychosis and der(18)t(5;18)(p14.1;p11.23).Semantic proximity Read ↗

Molecular and clinical characterization of a recurrent cryptic unbalanced t(4q;18q) resulting in an 18q deletion and 4q duplication.Semantic proximity Read ↗

Genotype-phenotype mapping of chromosome 18q deletions by high-resolution array CGH: an update of the phenotypic map.Semantic proximity Read ↗

High-resolution SNP microarray investigation of copy number variations on chromosome 18 in a control cohort.Semantic proximity Read ↗

Craniofacial and Neurological Phenotype in a Patient with De Novo 18q Microdeletion and 18p Microduplication.Semantic proximity Read ↗

Clinical and genomic profiling of a patient with a de novo ring chromosome 18: A case report highlighting autoimmune and neurological implicationsSemantic proximity Read ↗

Inherited duplication of the short arm of chromosome 18p11.32–p11.31 associated with developmental delay/intellectual disabilitySemantic proximity Read ↗

Refining the 22q11.2 deletion breakpoints in DiGeorge syndrome by aCGHSemantic proximity Read ↗

Familial 4.8 MB deletion on 18q23 associated with growth hormone insufficiency and phenotypic variability.Semantic proximity Read ↗

Mosaic Ring Chromosome 18, Ring Chromosome 18 Duplication/Deletion and Disomy 18: Perinatal Findings and Molecular Cytogenetic Characterization by Fluorescence In Situ Hybridization and Array Comparative Genomic HybridizationSemantic proximity Read ↗

Molecular characterisation of a proximal chromosome 18q deletion.Semantic proximity Read ↗

Ring 18 molecular assessment and clinical consequences.Semantic proximity Read ↗

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