doi: 10.1136/adc.74.1.62.
Chromosome 22q11 microdeletions in tetralogy of Fallot
Affiliations
- PMID: 8660052
- PMCID: PMC1511583
- DOI: 10.1136/adc.74.1.62
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Chromosome 22q11 microdeletions in tetralogy of Fallot
Arch Dis Child.
1996 Jan.
Abstract
Chromosome 22q11 fluorescence in situ hybridisation (FISH) studies were performed on 33 consecutive individuals attending a paediatric cardiology clinic with tetralogy of Fallot. Seven children had 22q11 microdeletions but only four had other clinical features associated with the newly recognised chromosome 22 deletion syndrome (CATCH 22). Chromosome 22q11 FISH studies should therefore be performed on all patients with tetralogy of Fallot.
Comment in
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Chromosome 22q11 microdeletion and isolated conotruncal heart defects.Arch Dis Child. 1997 Jan;76(1):79-80. doi: 10.1136/adc.76.1.79a. Arch Dis Child. 1997. PMID: 9059172 Free PMC article. No abstract available.
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