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Article

Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus

1 May 1992

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

Identifiers

PMID: 1349369
DOI: 10.1016/0140-6736(92)90734-k

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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.

Related research

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Research trail→

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Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locusPMID 1349369Read ↗

Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromesSemantic proximity Read ↗

Chromosome 22q11.2 Deletion Syndrome: DiGeorge Syndrome/Velocardiofacial SyndromeSemantic proximity Read ↗

22q11.2 Distal Deletion: A Recurrent Genomic Disorder Distinct from DiGeorge Syndrome and Velocardiofacial SyndromeSemantic proximity Read ↗

The Diverse Clinical Features of Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome)Semantic proximity Read ↗

The 22q11.2 deletion syndrome.Semantic proximity Read ↗

A Novel 22q11.2 Microdeletion in DiGeorge SyndromeSemantic proximity Read ↗

The Philadelphia story: the 22q11.2 deletion: report on 250 patients.Semantic proximity Read ↗

Familial DiGeorge/velocardiofacial syndrome with deletions of chromosome area22q11.2: Report of five families with a review of the literatureSemantic proximity Read ↗

Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome.Semantic proximity Read ↗

Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndrome.Semantic proximity Read ↗

Velo-cardio-facial and partial DiGeorge phenotype in a child with interstitial deletion at 10p13--implications for cytogenetics and molecular biology.Semantic proximity Read ↗

Deletion 22q11: Spectrum of Associated DisordersSemantic proximity Read ↗

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