A Mutation in Mouse Pak1ip1 Causes Orofacial Clefting while Human PAK1IP1 Maps to 6p24 Translocation Breaking Points Associated with Orofacial Clefting

Orofacial clefts are among the most common birth defects and result in an improper formation of the mouth or the roof of the mouth. Monosomy of the distal aspect of human chromosome 6p has been recognized as causative in congenital malformations affecting the brain and cranial skeleton including oro...

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Detalles Bibliográficos
Autores principales: Ross, Adam P., Mansilla, M. Adela, Choe, Youngshik, Helminski, Simon, Sturm, Richard, Maute, Roy L., May, Scott R., Hozyasz, Kamil K., Wójcicki, Piotr, Mostowska, Adrianna, Davidson, Beth, Adamopoulos, Iannis E., Pleasure, Samuel J., Murray, Jeffrey C., Zarbalis, Konstantinos S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3723895/
https://www.ncbi.nlm.nih.gov/pubmed/23935987
http://dx.doi.org/10.1371/journal.pone.0069333

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