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Article

Exploring the 7p22.1 chromosome as a candidate region for autism.

Journal of biomedicine & biotechnology - 1 Jan 2010

Bayou Nadia, Belhadj Ahlem, Daoud Hussein, Briault Sylvain, Helayem M Bechir, Chaabouni Habiba, M'rad Ridha

Abstract excerpt

A high incidence of de novo chromosomal aberrations in a population of persons with autism suggests a causal relationship between certain chromosomal aberrations and the occurrence of autism. A previous study on a Tunisian boy carrying a t(7;16) translocation identified the 7p22.1 as a positional candidate region for autism on chromosome 7. The characterization of the chromosomal breakpoints helped us to identify...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 20414355
DOI: 10.1155/2010/423894
PMCID: PMC2856063

Genes

MMD2
RBAK

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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