Cite
Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndrome.
MLA
Wilson, Gabrielle R., et al. “Mutations in SH3PXD2B Cause Borrone Dermato-Cardio-Skeletal Syndrome.” European Journal of Human Genetics, vol. 22, no. 6, June 2014, pp. 741–47. EBSCOhost, https://doi.org/10.1038/ejhg.2013.229.
APA
Wilson, G. R., Sunley, J., Smith, K. R., Pope, K., Bromhead, C. J., Fitzpatrick, E., Di Rocco, M., van Steensel, M., Coman, D. J., Leventer, R. J., Delatycki, M. B., Amor, D. J., Bahlo, M., & Lockhart, P. J. (2014). Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndrome. European Journal of Human Genetics, 22(6), 741–747. https://doi.org/10.1038/ejhg.2013.229
Chicago
Wilson, Gabrielle R, Jasmine Sunley, Katherine R Smith, Kate Pope, Catherine J Bromhead, Elizabeth Fitzpatrick, Maja Di Rocco, et al. 2014. “Mutations in SH3PXD2B Cause Borrone Dermato-Cardio-Skeletal Syndrome.” European Journal of Human Genetics 22 (6): 741–47. doi:10.1038/ejhg.2013.229.