Cite
Expansion of phenotype and genotypic data in CRB2-related syndrome.
MLA
Lamont, Ryan E., et al. “Expansion of Phenotype and Genotypic Data in CRB2-Related Syndrome.” European Journal of Human Genetics : EJHG, vol. 24, no. 10, Oct. 2016, pp. 1436–44. EBSCOhost, https://doi.org/10.1038/ejhg.2016.24.
APA
Lamont, R. E., Tan, W.-H., Innes, A. M., Parboosingh, J. S., Schneidman-Duhovny, D., Rajkovic, A., Pappas, J., Altschwager, P., DeWard, S., Fulton, A., Gray, K. J., Krall, M., Mehta, L., Rodan, L. H., Saller, D. N., Jr, Steele, D., Stein, D., Yatsenko, S. A., Bernier, F. P., & Slavotinek, A. M. (2016). Expansion of phenotype and genotypic data in CRB2-related syndrome. European Journal of Human Genetics : EJHG, 24(10), 1436–1444. https://doi.org/10.1038/ejhg.2016.24
Chicago
Lamont, Ryan E, Wen-Hann Tan, A Micheil Innes, Jillian S Parboosingh, Dina Schneidman-Duhovny, Aleksandar Rajkovic, John Pappas, et al. 2016. “Expansion of Phenotype and Genotypic Data in CRB2-Related Syndrome.” European Journal of Human Genetics : EJHG 24 (10): 1436–44. doi:10.1038/ejhg.2016.24.