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Article

Molecular characterization of deletion breakpoints in adults with 22q11 deletion syndrome.

Human genetics - 1 Feb 2007

Weksberg Rosanna, Stachon Andrea C, Squire Jeremy A, Moldovan Laura, Bayani Jane, Meyn Stephen, Chow Eva, Bassett Anne S

Abstract excerpt

22q11 Deletion syndrome (22q11DS) is a common microdeletion syndrome with variable expression, including congenital and later onset conditions such as schizophrenia. Most studies indicate that expression does not appear to be related to length of the deletion but there is limited information on t...

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Share to Chromosome Breakage
Share to Chromosome Deletion
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 22

Share to In Situ Hybridization, Fluorescence

Share to Repetitive Sequences, Nucleic Acid

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Source

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Identifiers

PMID: 17028864
DOI: 10.1007/s00439-006-0242-x
PMCID: PMC3139629

Genes

PRODH
COMT
TBX1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17028864-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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