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Chromosomal abnormalities among children born with conotruncal cardiac defects
BACKGROUND: Conotruncal heart defects comprise 25%-30% of non-syndromic congenital heart defects. This study describes the frequency of chromosome abnormalities and microdeletion 22q11 associated with conotruncal heart malformations. METHODS: From a population base of 974,579 infants/fetuses deliver...
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| 主要な著者: | , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2009
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2856481/ https://ncbi.nlm.nih.gov/pubmed/19067405 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/bdra.20541 |
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