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Article

Detection and characterization of copy number variation in autism spectrum disorder.

Methods in molecular biology (Clifton, N.J.) - 1 Jan 2012

Marshall Christian R, Scherer Stephen W

Abstract excerpt

There now exist multiple lines of evidence pointing to a significant genetic component underlying the aetiology of autism spectrum disorders (ASDs). The advent of methodologies for scanning the human genome at high resolution, coupled with the recognition of copy number variation (CNV) as a prevalent source of genomic variation, has led to new strategies in the identification of clinically relevant loci. Balanced...

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Share to Autistic Disorder
Share to DNA Copy Number Variations
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Polymorphism, Single Nucleotide

Source

Identifiers

PMID: 22228009
DOI: 10.1007/978-1-61779-507-7_5

Genes

NRXN1
PTCHD1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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