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Article

A Bronchovascular Anomaly in a Patient With 22q11.2 Deletion Syndrome.

Journal of investigational allergology & clinical immunology - 1 Jan 2000

Romano R, Cirillo E, Giardino G, Gallo V, Mollica C, Pignata C

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Share to Abnormalities, Multiple
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 27996952
DOI: 10.18176/jiaci.0107

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Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A Bronchovascular Anomaly in a Patient With 22q11.2 Deletion Syndrome.PMID 27996952Read ↗

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

5q11.2 deletion in a patient with tracheal agenesisSemantic proximity Read ↗

Bilateral persistent fetal vasculature and a chromosome 10 mutation including COX15.Semantic proximity Read ↗

Lethal renal anomalies in a fetus with 21q22.11-q22.12 deletion.Semantic proximity Read ↗

Laryngeal abnormalities are frequent in the 22q11 deletion syndromeSemantic proximity Read ↗

Frequent association of 22q11.2 deletion with tetralogy of FallotSemantic proximity Read ↗

D-transposition of the great arteries in a case of microduplication 22q11.2.Semantic proximity Read ↗

Three patients with different phenotypes in a family with chromosome 22q11.2 deletions.Semantic proximity Read ↗

Tetralogy of fallot with pulmonary atresia associated with chromosome 22q11 deletionSemantic proximity Read ↗

Laryngeal atresia type III (glottic web) with 22q11.2 microdeletion: Report of three patientsSemantic proximity Read ↗

Prenatal diagnosis of an unexpected interstitial 22q11.2 deletion causing truncus arteriosus and thymic hypoplasia in a ring 22 chromosome derived from a maternally inherited paracentric inversionSemantic proximity Read ↗

Pulmonary agenesis: expansion of the VCFS phenotype.Semantic proximity Read ↗

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