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Extracardiac features predicting 22q11.2 Deletion Syndrome in adult congenital heart disease
BACKGROUND AND OBJECTIVES: 22q11.2 Deletion Syndrome (22q11.2DS) is an important genetic syndrome to cardiologists yet remains under-recognized in adults. There is no evidence-based guideline for genetic testing referrals. Feasibility issues in many jurisdictions preclude testing for 22q11.2 deletio...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3139626/ https://ncbi.nlm.nih.gov/pubmed/18191243 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ijcard.2007.08.141 |
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