De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.

MLA

Burrage, Lindsay C., et al. “De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.” American Journal of Human Genetics, vol. 97, no. 6, Dec. 2015, pp. 904–13. EBSCOhost, https://doi.org/10.1016/j.ajhg.2015.11.006.

APA

Burrage, L. C., Charng, W.-L., Eldomery, M. K., Willer, J. R., Davis, E. E., Lugtenberg, D., Zhu, W., Leduc, M. S., Akdemir, Z. C., Azamian, M., Zapata, G., Hernandez, P. P., Schoots, J., de Munnik, S. A., Roepman, R., Pearring, J. N., Jhangiani, S., Katsanis, N., Vissers, L. E. L. M., & Brunner, H. G. (2015). De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. American Journal of Human Genetics, 97(6), 904–913. https://doi.org/10.1016/j.ajhg.2015.11.006

Chicago

Burrage, Lindsay C., Wu-Lin Charng, Mohammad K. Eldomery, Jason R. Willer, Erica E. Davis, Dorien Lugtenberg, Wenmiao Zhu, et al. 2015. “De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.” American Journal of Human Genetics 97 (6): 904–13. doi:10.1016/j.ajhg.2015.11.006.