Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar Atrophy.

MLA

Harel, Tamar, et al. “Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar Atrophy.” American Journal of Human Genetics, vol. 98, no. 3, Mar. 2016, pp. 562–70. EBSCOhost, https://doi.org/10.1016/j.ajhg.2016.01.011.

APA

Harel, T., Yesil, G., Bayram, Y., Coban-Akdemir, Z., Charng, W.-L., Karaca, E., Al Asmari, A., Eldomery, M. K., Hunter, J. V., Jhangiani, S. N., Rosenfeld, J. A., Pehlivan, D., El-Hattab, A. W., Saleh, M. A., LeDuc, C. A., Muzny, D., Boerwinkle, E., Gibbs, R. A., Chung, W. K., … Lupski, J. R. (2016). Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar Atrophy. American Journal of Human Genetics, 98(3), 562–570. https://doi.org/10.1016/j.ajhg.2016.01.011

Chicago

Harel, Tamar, Gozde Yesil, Yavuz Bayram, Zeynep Coban-Akdemir, Wu-Lin Charng, Ender Karaca, Ali Al Asmari, et al. 2016. “Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar Atrophy.” American Journal of Human Genetics 98 (3): 562–70. doi:10.1016/j.ajhg.2016.01.011.