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Identification of clinically relevant phenotypes in patients with Ebstein anomaly
BACKGROUND: Ebstein anomaly (EA) is a heterogeneous congenital heart defect (CHD), frequently accompanied by diverse cardiac and extracardiac comorbidities, resulting in a wide range of clinical outcomes. HYPOTHESIS: Phenotypic characterization of EA patients has the potential to identify variables...
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| Veröffentlicht in: | Clin Cardiol |
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| Hauptverfasser: | , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Wiley Periodicals, Inc.
2018
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6489938/ https://ncbi.nlm.nih.gov/pubmed/29569399 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/clc.22870 |
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