Complex Congenital Heart Disease in Unaffected Relatives of Adults With 22q11.2 Deletion Syndrome

The 22.q11.2 deletion syndrome (22q11DS) is a common genetic condition associated with 22q11.2 microdeletions and classically has included congenital heart disease (CHD) as a part of the variable expression. Some evidence has shown that relatives of those with 22q11DS might be at an increased risk o...

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Bibliographische Detailangaben
Hauptverfasser: Swaby, Jodi-Ann M., Silversides, Candice K., Bekeschus, Sean C., Piran, Sara, Oechslin, Erwin N., Chow, Eva W. C., Bassett, Anne S.
Format: Artigo
Sprache:Inglês
Veröffentlicht: 2011
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Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3188300/
https://ncbi.nlm.nih.gov/pubmed/21257016
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.amjcard.2010.09.045
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