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 evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities

1 Sept 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 Autism Spectrum Disorder Research
Share to Down syndrome and intellectual disability research
Share to Genomic variations and chromosomal abnormalities

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 21844811
DOI: 10.1097/gim.0b013e31822c79f9

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilitiesPMID 21844811Read ↗

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

Gene copy number variation and common human disease.Semantic proximity Read ↗

Human genes involved in copy number variation: mechanisms of origin, functional effects and implications for disease.Semantic proximity Read ↗

Structural genomic variation in intellectual disability.Semantic proximity Read ↗

Gene discovery and functional assessment of rare copy-number variants in neurodevelopmental disorders.Semantic proximity Read ↗

A commentary on implication of gene copy number variation in health and diseases.Semantic proximity Read ↗

The impact of human copy number variation on a new era of genetic testingSemantic proximity Read ↗

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

Copy-number variations associated with neuropsychiatric conditions.Semantic proximity Read ↗

Human copy number variation and complex genetic disease.Semantic proximity Read ↗

Characteristics and mode of inheritance of pathogenic copy number variants in prenatal diagnosisSemantic proximity Read ↗

Copy number variations in the human genome and strategies for analysis.Semantic proximity Read ↗

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