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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...
Tallennettuna:
| Päätekijät: | , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2011
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| Aiheet: | |
| Linkit: | 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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