APA (7th ed.) Citation

Schrauwen, I., Kari, E., Mattox, J., Llaci, L., Smeeton, J., Naymik, M., . . . Friedman, R. A. (2018). De novo variants in GREB1L are associated with non-syndromic inner ear malformations and deafness. Human genetics, 137(6-7), 459-470. https://doi.org/10.1007/s00439-018-1898-8

Chicago Style (17th ed.) Citation

Schrauwen, Isabelle, et al. "De Novo Variants in GREB1L Are Associated with Non-syndromic Inner Ear Malformations and Deafness." Human Genetics 137, no. 6-7 (2018): 459-470. https://doi.org/10.1007/s00439-018-1898-8.

MLA (9th ed.) Citation

Schrauwen, Isabelle, et al. "De Novo Variants in GREB1L Are Associated with Non-syndromic Inner Ear Malformations and Deafness." Human Genetics, vol. 137, no. 6-7, 2018, pp. 459-470, https://doi.org/10.1007/s00439-018-1898-8.