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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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Detalles Bibliográficos
Publicado en:Cell Rep
Main Authors: Wilderman, Andrea, VanOudenhove, Jennifer, Kron, Jeffrey, Noonan, James P., Cotney, Justin
Formato: Artigo
Idioma:Inglês
Publicado: 2018
Assuntos:
Acceso en liña: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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