PBX-WNT-P63-IRF6 pathway in nonsyndromic cleft lip and palate

Nonsyndromic cleft lip and palate (NSCLP) is one of the most common craniofacial anomalies in humans, affecting more than 135,000 newborns worldwide. NSCLP has a multifactorial etiology with more than 50 genes postulated to play an etiologic role. The genetic pathway comprised of Pbx-Wnt-p63-Irf6 ge...

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Dades bibliogràfiques
Publicat a:Birth Defects Res
Autors principals: Maili, Lorena, Letra, Ariadne, Silva, Renato, Buchanan, Edward P., Mulliken, J.B., Greives, M.R., Teichgraeber, J.F., Blackwell, S.J., Ummer, Rohit, Weber, Ryan, Chiquet, Brett, Blanton, Susan H., Hecht, Jacqueline T.
Format: Artigo
Idioma:Inglês
Publicat: 2019
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7325739/
https://ncbi.nlm.nih.gov/pubmed/31825181
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/bdr2.1630
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