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Evaluation of Potential Modifiers of the Cardiac Phenotype in the 22q11.2 Deletion Syndrome
BACKGROUND: The phenotype associated with deletion of the 22q11.2 chromosomal region is highly variable, yet little is known about the source of this variability. Cardiovascular anomalies, including tetralogy of Fallot, truncus arteriosus, interrupted aortic arch type B, perimembranous ventricular s...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2810963/ https://ncbi.nlm.nih.gov/pubmed/18770859 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/bdra.20501 |
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