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Article

Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder.

BMC medical genetics - 18 Jan 2005

Reddy Kavita S

Abstract excerpt

BACKGROUND: Autism is a behavioral disorder with impaired social interaction, communication, and repetitive and stereotypic behaviors. About 5-10 % of individuals with autism have 'secondary' autism in which an environmental agent, chromosome abnormality, or single gene disorder can be identified. Ninety percent have idiopathic autism and a major gene has not yet been identified. We have assessed the incidence of...

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Share to Autistic Disorder
Share to Chromosome Aberrations
Share to Cytogenetic Analysis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fragile X Mental Retardation Protein

Share to Fragile X Syndrome

Share to Molecular Epidemiology

Share to Nerve Tissue Proteins

Share to RNA-Binding Proteins

Source

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Identifiers

PMID: 15655077
DOI: 10.1186/1471-2350-6-3
PMCID: PMC548305

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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