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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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Bibliografiske detaljer
Main Authors: Goldmuntz, Elizabeth, Driscoll, Deborah A., Emanuel, Beverly S., McDonald-McGinn, Donna, Mei, Minghua, Zackai, Elaine, Mitchell, Laura E.
Format: Artigo
Sprog:Inglês
Udgivet: 2009
Fag:
Online adgang: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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