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Article

A region of homozygosity within 22q11.2 associated with congenital heart disease: recessive DiGeorge/velocardiofacial syndrome?

Journal of medical genetics - 1 Aug 2001

Henwood J, Pickard C, Leek J P, Bennett C P, Crow Y J, Thompson J D, Ahmed M, Watterson K G, Parsons J M, Roberts E, Lench N J

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Share to Abnormalities, Multiple
Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 22

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Consanguinity

Share to Craniofacial Abnormalities

Share to DiGeorge Syndrome

Share to Fatal Outcome

Share to Heart Defects, Congenital

Source

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Identifiers

PMID: 11494964
DOI: 10.1136/jmg.38.8.533
PMCID: PMC1734916

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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A region of homozygosity within 22q11.2 associated with congenital heart disease: recessive DiGeorge/velocardiofacial syndrome?PMID 11494964Read ↗

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