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

Genomic profile of copy number variants on the short arm of human chromosome 8

12 May 2010

Abstract excerpt

No abstract is available from the source.

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

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 20461109
DOI: 10.1038/ejhg.2010.66

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genomic profile of copy number variants on the short arm of human chromosome 8PMID 20461109Read ↗

Origins and functional impact of copy number variation in the human genome.Semantic proximity Read ↗

Genomic copy number variation, human health, and disease.Semantic proximity Read ↗

Large-scale copy number polymorphism in the human genome.Semantic proximity Read ↗

Copy number variation in the human genome and its implications for cardiovascular disease.Semantic proximity Read ↗

Genome-wide Association of Copy-Number Variation Reveals an Association between Short Stature and the Presence of Low-Frequency Genomic DeletionsSemantic proximity Read ↗

Copy-number variations add a new layer of complexity in the human genome.Semantic proximity Read ↗

Exon Array CGH: Detection of Copy-Number Changes at the Resolution of Individual Exons in the Human GenomeSemantic proximity Read ↗

American College of Medical Genetics recommendations for the design and performance expectations for clinical genomic copy number microarrays intended for use in the postnatal setting for detection of constitutional abnormalitiesSemantic proximity Read ↗

Copy Number Variants, Aneuploidies, and Human DiseaseSemantic proximity Read ↗

Structural variation in the human genome: the impact of copy number variants on clinical diagnosis.Semantic proximity Read ↗

Strategies for the detection of copy number and other structural variants in the human genome.Semantic proximity Read ↗

Side effects of genome structural changes.Semantic proximity Read ↗

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