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Article

DiGeorge syndrome: an historical review of clinical and cytogenetic features.

1 Oct 1993

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Source

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

Identifiers

PMID: 8230154
DOI: 10.1136/jmg.30.10.803

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.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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DiGeorge syndrome: an historical review of clinical and cytogenetic features.PMID 8230154Read ↗

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The evaluation of DiGeorge syndrome gene deletion using molecular cytogenetic techniquesSemantic proximity Read ↗

[Clinical findings and immunologic variability in 9 patients with DiGeorge syndrome].Semantic proximity Read ↗

Chromosome 22q11.2 Deletion (DiGeorge Syndrome): Immunologic Features, Diagnosis, and ManagementSemantic proximity Read ↗

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

Characterization of 10p Deletions Suggests Two Nonoverlapping Regions Contribute to the DiGeorge Syndrome PhenotypeSemantic proximity Read ↗

DiGeorge syndrome with discordant phenotype in monozygotic twins.Semantic proximity Read ↗

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