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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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Bibliografske podrobnosti
izdano v:Cell Rep
Main Authors: Wilderman, Andrea, VanOudenhove, Jennifer, Kron, Jeffrey, Noonan, James P., Cotney, Justin
Format: Artigo
Jezik:Inglês
Izdano: 2018
Teme:
Online dostop: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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