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High-Resolution Epigenomic Atlas of Human Embryonic Craniofacial Development
Defects in patterning during human embryonic development frequently result in craniofacial abnormalities. The gene regulatory programs that build the craniofacial complex are likely controlled by information located between genes and within intronic sequences. However, systematic identification of r...
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| 出版年: | Cell Rep |
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| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2018
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5965702/ https://ncbi.nlm.nih.gov/pubmed/29719267 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.celrep.2018.03.129 |
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