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Oligogenic Effects of 16p11.2 Copy-Number Variation on Craniofacial Development

A copy-number variant (CNV) of 16p11.2 encompassing 30 genes is associated with developmental and psychiatric disorders, head size, and body mass. The genetic mechanisms that underlie these associations are not understood. To determine the influence of 16p11.2 genes on development, we investigated t...

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Detalles Bibliográficos
Autores principales:	Qiu, Yuqi, Arbogast, Thomas, Lorenzo, Sandra Martin, Li, Hongying, Tang, Shih C., Richardson, Ellen, Hong, Oanh, Cho, Shawn, Shanta, Omar, Pang, Timothy, Corsello, Christina, Deutsch, Curtis K., Chevalier, Claire, Davis, Erica E., lakoucheva, Lilia M., Herault, Yann, Katsanis, Nicholas, Messer, Karen, Sebat, Jonathan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	2019
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6988705/ https://www.ncbi.nlm.nih.gov/pubmed/31553903 http://dx.doi.org/10.1016/j.celrep.2019.08.071

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