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

Genome-wide Association of Copy-Number Variation Reveals an Association between Short Stature and the Presence of Low-Frequency Genomic Deletions

23 Nov 2011

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 Genomic variations and chromosomal abnormalities
Share to Genomics and Rare Diseases
Share to Prenatal Screening and Diagnostics

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 22118881
DOI: 10.1016/j.ajhg.2011.10.014

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

Genome-wide Association of Copy-Number Variation Reveals an Association between Short Stature and the Presence of Low-Frequency Genomic DeletionsPMID 22118881Read ↗

Rare copy number variants are a common cause of short stature.Semantic proximity Read ↗

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

Copy number variants in patients with short stature.Semantic proximity Read ↗

Mutational and selective effects on copy-number variants in the human genome.Semantic proximity Read ↗

Genomic profile of copy number variants on the short arm of human chromosome 8Semantic proximity Read ↗

Copy number variants in short children born small for gestational age.Semantic proximity Read ↗

An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilitiesSemantic proximity Read ↗

Large multiallelic copy number variations in humans.Semantic proximity Read ↗

The functional impact of copy number variation in the human genomeSemantic proximity Read ↗

Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen)Semantic proximity Read ↗

Analysis of Population-Genetic Properties of Copy Number Variations.Semantic proximity Read ↗

Recurrent Copy Number Variants Associated with Syndromic Short Stature of Unknown Cause.Semantic proximity Read ↗

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