De novo truncating variants in PHF21A cause intellectual disability and craniofacial anomalies.

MLA

Hamanaka, Kohei, et al. “De Novo Truncating Variants in PHF21A Cause Intellectual Disability and Craniofacial Anomalies.” European Journal of Human Genetics : EJHG, vol. 27, no. 3, Mar. 2019, pp. 378–83. EBSCOhost, https://doi.org/10.1038/s41431-018-0289-x.

APA

Hamanaka, K., Sugawara, Y., Shimoji, T., Nordtveit, T. I., Kato, M., Nakashima, M., Saitsu, H., Suzuki, T., Yamakawa, K., Aukrust, I., Houge, G., Mitsuhashi, S., Takata, A., Iwama, K., Alkanaq, A., Fujita, A., Imagawa, E., Mizuguchi, T., Miyake, N., … Matsumoto, N. (2019). De novo truncating variants in PHF21A cause intellectual disability and craniofacial anomalies. European Journal of Human Genetics : EJHG, 27(3), 378–383. https://doi.org/10.1038/s41431-018-0289-x

Chicago

Hamanaka, Kohei, Yuji Sugawara, Takeyoshi Shimoji, Tone Irene Nordtveit, Mitsuhiro Kato, Mitsuko Nakashima, Hirotomo Saitsu, et al. 2019. “De Novo Truncating Variants in PHF21A Cause Intellectual Disability and Craniofacial Anomalies.” European Journal of Human Genetics : EJHG 27 (3): 378–83. doi:10.1038/s41431-018-0289-x.