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Article

A 2-Mb critical region implicated in the microcephaly associated with terminal 1q deletion syndrome.

American journal of medical genetics. Part A - 1 Aug 2007

Hill Anthony D, Chang Bernard S, Hill R Sean, Garraway Levi A, Bodell Adria, Sellers William R, Walsh Christopher A

Abstract excerpt

Patients with distal deletions of chromosome 1q have a recognizable syndrome that includes microcephaly, hypoplasia or agenesis of the corpus callosum, and psychomotor retardation. Although these symptoms have been attributed to deletions of 1q42-1q44, the minimal chromosomal region involved has not been identified. Using microsatellite and single nucleotide polymorphism (SNP) markers, we have mapped the deleted...

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Share to Agenesis of Corpus Callosum
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 17603806
DOI: 10.1002/ajmg.a.31776

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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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A 2-Mb critical region implicated in the microcephaly associated with terminal 1q deletion syndrome.PMID 17603806Read ↗

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