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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Anat Rec (Hoboken)
Autors principals: Badri, Mohammed K., Zhang, Honghao, Ohyama, Yoshio, Venkitapathi, Sundharamani, Kamiya, Nobuhiro, Takeda, Haruko, Ray, Manas, Scott, Greg, Tsuji, Takehito, Kunieda, Tetsuo, Mishina, Yuji, Mochida, Yoshiyuki
Format: Artigo
Idioma:Inglês
Publicat: 2016
Matèries:
Article
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars