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Article

The Diverse Clinical Features of Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome)

9 Oct 2013

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

Identifiers

PMID: 24565705
DOI: 10.1016/j.jaip.2013.08.003

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

The Diverse Clinical Features of Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome)PMID 24565705Read ↗

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

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

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

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

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

Clinical Manifestations of 22q11.2 Deletion SyndromeSemantic proximity Read ↗

Immune and Genetic Features of the Chromosome 22q11.2 Deletion (DiGeorge Syndrome)Semantic proximity Read ↗

DiGeorge syndrome: an historical review of clinical and cytogenetic features.Semantic proximity Read ↗

Chromosome 22q11.2 deletion syndrome (DiGeorge and velocardiofacial syndromes).Semantic proximity Read ↗

Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locusSemantic proximity Read ↗

Review of the Pathophysiology and Clinical Manifestations of 22q11.2 Deletion and Duplication SyndromesSemantic proximity Read ↗

The 22q11.2 deletion syndrome: Cancer predisposition, platelet abnormalities and cytopenias.Semantic proximity Read ↗

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