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Ellis van Creveld2 is required for postnatal craniofacial bone development
Ellis-van Creveld (EvC) syndrome is a genetic disorder with mutations in either EVC or EVC2 gene. Previous case studies reported that EvC patients underwent orthodontic treatment, suggesting the presence of craniofacial bone phenotypes. To investigate whether a mutation in EVC2 gene causes a craniof...
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| Publicado no: | Anat Rec (Hoboken) |
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| Main Authors: | , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4940231/ https://ncbi.nlm.nih.gov/pubmed/27090777 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ar.23353 |
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