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Article

Three phases of DiGeorge/22q11 deletion syndrome pathogenesis during brain development: patterning, proliferation, and mitochondrial functions of 22q11 genes.

International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience - 1 May 2011

Meechan D W, Maynard T M, Tucker E S, LaMantia A-S

Abstract excerpt

DiGeorge, or 22q11 deletion syndrome (22q11DS), the most common survivable human genetic deletion disorder, is caused by deletion of a minimum of 32 contiguous genes on human chromosome 22, and presumably results from diminished dosage of one, some, or all of these genes--particularly during deve...

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Identifiers

PMID: 20833244
DOI: 10.1016/j.ijdevneu.2010.08.005
PMCID: PMC3770287

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20833244-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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