APA (7th ed.) Citation

Rad, A., Altunoglu, U., Miller, R., Maroofian, R., James, K. N., Çağlayan, A. O., . . . Schmidts, M. (2019). MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive cerebellar, ocular, craniofacial and genital features (COFG syndrome). Journal of medical genetics, 56(5), 332-339. https://doi.org/10.1136/jmedgenet-2018-105623

Chicago Style (17th ed.) Citation

Rad, Abolfazl, et al. "MAB21L1 Loss of Function Causes a Syndromic Neurodevelopmental Disorder with Distinctive Cerebellar, Ocular, Craniofacial and Genital Features (COFG Syndrome)." Journal of Medical Genetics 56, no. 5 (2019): 332-339. https://doi.org/10.1136/jmedgenet-2018-105623.

MLA (9th ed.) Citation

Rad, Abolfazl, et al. "MAB21L1 Loss of Function Causes a Syndromic Neurodevelopmental Disorder with Distinctive Cerebellar, Ocular, Craniofacial and Genital Features (COFG Syndrome)." Journal of Medical Genetics, vol. 56, no. 5, 2019, pp. 332-339, https://doi.org/10.1136/jmedgenet-2018-105623.