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Microdeletions and Microduplications in Patients with Congenital Heart Disease and Multiple Congenital Anomalies
OBJECTIVE: Multiple genetic syndromes are caused by recurrent chromosomal microdeletions or microduplications. The increasing use of high-resolution microarrays in clinical analysis has allowed the identification of previously undetectable submicroscopic copy number variants (CNVs) associated with g...
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| 出版年: | Congenit Heart Dis |
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| 主要な著者: | , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2011
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4575121/ https://ncbi.nlm.nih.gov/pubmed/22010865 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1747-0803.2011.00582.x |
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