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13q13.1–q13.2 deletion in tetralogy of Fallot: Clinical report and a literature review
Recent advances in microarray technology are helping to identify more genetic anomalies associated with tetralogy of Fallot and other congenital heart defects. We report on a 24-year-old woman with a syndromic form of tetralogy of Fallot who was found to have a novel de novo deletion of the proximal...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3295832/ https://ncbi.nlm.nih.gov/pubmed/20598760 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ijcard.2010.05.070 |
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