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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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| Publicat a: | Cell Rep |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2018
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| Matèries: | |
| Accés en línia: | 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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