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Evidence for craniofacial enhancer variation underlying nonsyndromic cleft lip and palate
Nonsyndromic cleft lip with or without cleft palate (NSCLP) is a common birth defect for which only ~20% of the underlying genetic variation has been identified. Variants in noncoding regions have been increasingly suggested to contribute to the missing heritability. In this study, we investigated w...
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| 出版年: | Hum Genet |
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| 主要な著者: | , , , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2020
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7487053/ https://ncbi.nlm.nih.gov/pubmed/32318854 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-020-02169-9 |
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