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Identification of novel genomic imbalances in Saudi patients with congenital heart disease
BACKGROUND: Quick genetic diagnosis of a patient with congenital heart disease (CHD) is quite important for proper health care and management. Copy number variations (CNV), chromosomal imbalances and rearrangements have been frequently associated with CHD. Previously, due to limitations of microscop...
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| 出版年: | Mol Cytogenet |
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| 主要な著者: | , , , , , , , , , , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2018
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| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5784682/ https://ncbi.nlm.nih.gov/pubmed/29416564 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-018-0356-6 |
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