Cite
Whole-exome sequencing links TMCO1 defect syndrome with cerebro-facio-thoracic dysplasia.
MLA
Pehlivan, Davut, et al. “Whole-Exome Sequencing Links TMCO1 Defect Syndrome with Cerebro-Facio-Thoracic Dysplasia.” European Journal of Human Genetics, vol. 22, no. 9, Sept. 2014, pp. 1145–48. EBSCOhost, https://doi.org/10.1038/ejhg.2013.291.
APA
Pehlivan, D., Karaca, E., Aydin, H., Beck, C. R., Gambin, T., Muzny, D. M., Bilge Geckinli, B., Karaman, A., Jhangiani, S. N., Gibbs, R. A., & Lupski, J. R. (2014). Whole-exome sequencing links TMCO1 defect syndrome with cerebro-facio-thoracic dysplasia. European Journal of Human Genetics, 22(9), 1145–1148. https://doi.org/10.1038/ejhg.2013.291
Chicago
Pehlivan, Davut, Ender Karaca, Hatip Aydin, Christine R Beck, Tomasz Gambin, Donna M Muzny, B Bilge Geckinli, et al. 2014. “Whole-Exome Sequencing Links TMCO1 Defect Syndrome with Cerebro-Facio-Thoracic Dysplasia.” European Journal of Human Genetics 22 (9): 1145–48. doi:10.1038/ejhg.2013.291.