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Aortic Root Dilation in Patients With 22q11.2 Deletion Syndrome
The 22q11.2 deletion syndrome is characterized by a highly variable phenotype including a range of cardiac malformations. The most common cardiovascular features include a subset of conotruncal defects, perimembranous ventricular septal defects and aortic arch anomalies. This report describes a seri...
Bewaard in:
| Hoofdauteurs: | , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2009
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4080309/ https://ncbi.nlm.nih.gov/pubmed/19353635 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.32770 |
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