Carregant...
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...
Guardat en:
| Autors principals: | , , , |
|---|---|
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2009
|
| Matèries: | |
| Accés en línia: | 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 |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|