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Functional consequences of copy number variants in miscarriage
BACKGROUND: The presence of unique copy number variations (CNVs) in miscarriages suggests that their integral genes have a role in maintaining early pregnancy. In our previous work, we identified 19 unique CNVs in ~40% of studied euploid miscarriages, which were predominantly familial in origin. In...
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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
2015
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4324423/ https://ncbi.nlm.nih.gov/pubmed/25674159 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-015-0109-8 |
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