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Calvarial osteoblast gene expression in patients with craniosynostosis leads to novel polygenic mouse model
Craniosynostosis is the premature fusion of the sutures of the calvaria and is principally designated as being either syndromic (demonstrating characteristic extracranial malformations) or non-syndromic. While many forms of syndromic craniosynostosis are known to be caused by specific mutations, the...
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| Publicado no: | PLoS One |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6707563/ https://ncbi.nlm.nih.gov/pubmed/31442251 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0221402 |
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