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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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| Publicado no: | Cell Rep |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2018
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| Assuntos: | |
| Acesso em linha: | 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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