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Article

22q11 DS: genomic mechanisms and gene function in DiGeorge/velocardiofacial syndrome.

International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience - 1 Jan 2000

Maynard Thomas M, Haskell Gloria T, Lieberman Jeffrey A, LaMantia Anthony-Samuel

Abstract excerpt

22q11 deletion syndrome (22qDS), also known as DiGeorge or velocardiofacial syndrome (DGS/VCFS), is a relatively common genetic anomaly that results in malformations of the heart, face and limbs. In addition, patients with 22qDS are at significant risk for psychiatric disorders as well, with one in four developing schizophrenia, and one in six developing major depressive disorders. Like several other deletion...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 12175881
DOI: 10.1016/s0736-5748(02)00050-3

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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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