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Article

[Extra-cardiac phenotype associated with microdeletion 22q11].

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie - 1 May 2002

Lacombe D

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

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Kidney

Share to Limb Deformities, Congenital

Share to Phenotype

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Identifiers

PMID: 12108232
DOI: 10.1016/s0929-693x(01)00908-3

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

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Research trail→

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[Extra-cardiac phenotype associated with microdeletion 22q11].PMID 12108232Read ↗

[Molecular basis of microdeletion 22q11].Semantic proximity Read ↗

Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well‐established knowledge to new frontiersSemantic proximity Read ↗

[X-linked dilated cardiomyopathy: a cardiospecific phenotype of dystrophinopathy].Semantic proximity Read ↗

[Analysis of microdeletions in 22q11 in Colombian patients with congenital heart disease].Semantic proximity Read ↗

[Chromosome 22 (22q.11.2) deletion. Etiology of conotruncal heart abnormalities].Semantic proximity Read ↗

Extracardiac features predicting 22q11.2 Deletion Syndrome in adult congenital heart diseaseSemantic proximity Read ↗

Cardiovascular Anomalies Associated With Chromosome 22q11.2 Deletion SyndromeSemantic proximity Read ↗

[Gene errors of dilated cardiomyopathy].Semantic proximity Read ↗

Heart defects and other features of the 22q11 distal deletion syndrome.Semantic proximity Read ↗

[Review of 22 patients with 22q11.2 deletion syndrome: phenotype spectrum].Semantic proximity Read ↗

The 22q11.2 deletion: from diversity to a single gene theory.Semantic proximity Read ↗

[Genotype and phenotype studies on fetuses of 22q11.2 deletion syndrome].Semantic proximity Read ↗

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