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Sox9 function in craniofacial development and disease
The Sox family of transcriptional regulators has been implicated in the control of a broad array of developmental processes. One member of this family SOX9 was first identified as a candidate gene for campomelic dysplasia (CD), a human syndrome affecting skeletal and testis development. In these pat...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3079054/ https://ncbi.nlm.nih.gov/pubmed/21309066 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/dvg.20717 |
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