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Article

Complete DiGeorge syndrome associated with CHD7 mutation.

The Journal of allergy and clinical immunology - 1 Oct 2007

Sanka Madhurima, Tangsinmankong Nutthapong, Loscalzo Melissa, Sleasman John W, Dorsey Morna J

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Topics

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 17931565
DOI: 10.1016/j.jaci.2007.08.013

Genes

CHD7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Complete DiGeorge syndrome associated with CHD7 mutation.PMID 17931565Read ↗

Gene symbol: CHD7. Disease: CHARGE syndrome.Semantic proximity Read ↗

CHARGE syndrome and CHD7 gene mutation.Semantic proximity Read ↗

DiGeorge's syndrome: a gene at last.Semantic proximity Read ↗

Genetic dissection of the DiGeorge syndrome phenotype.Semantic proximity Read ↗

CHARGE syndrome: a review.Semantic proximity Read ↗

DiGeorge Syndrome: New InsightsSemantic proximity Read ↗

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

Mutation update on the CHD7 gene involved in CHARGE syndrome.Semantic proximity Read ↗

Identification of two novel splice-site mutations in CHD7 gene in two patients with classical and atypical CHARGE syndrome phenotype.Semantic proximity Read ↗

[Mutation analysis of the CHD7 gene in patients with congenital heart disease].Semantic proximity Read ↗

CHD7 mutations are not a major cause of atrioventricular septal and conotruncal heart defects.Semantic proximity Read ↗

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

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