A relatively mild skeletal ciliopathy phenotype consistent with cranioectodermal dysplasia is associated with a homozygous nonsynonymous mutation in WDR35.

MLA

Smith, Christopher, et al. “A Relatively Mild Skeletal Ciliopathy Phenotype Consistent with Cranioectodermal Dysplasia Is Associated with a Homozygous Nonsynonymous Mutation in WDR35.” American Journal of Medical Genetics. Part A, vol. 170, no. 3, Mar. 2016, pp. 760–65. EBSCOhost, https://doi.org/10.1002/ajmg.a.37514.

APA

Smith, C., Lamont, R. E., Wade, A., Bernier, F. P., Parboosingh, J. S., & Innes, A. M. (2016). A relatively mild skeletal ciliopathy phenotype consistent with cranioectodermal dysplasia is associated with a homozygous nonsynonymous mutation in WDR35. American Journal of Medical Genetics. Part A, 170(3), 760–765. https://doi.org/10.1002/ajmg.a.37514

Chicago

Smith, Christopher, Ryan E Lamont, Andrew Wade, Francois P Bernier, Jillian S Parboosingh, and A Micheil Innes. 2016. “A Relatively Mild Skeletal Ciliopathy Phenotype Consistent with Cranioectodermal Dysplasia Is Associated with a Homozygous Nonsynonymous Mutation in WDR35.” American Journal of Medical Genetics. Part A 170 (3): 760–65. doi:10.1002/ajmg.a.37514.