APA (7th ed.) Citation

Knapp, K. M., Sullivan, R., Murray, J., Gimenez, G., Arn, P., D'Souza, P., . . . Bicknell, L. S. (2020). Linked-read genome sequencing identifies biallelic pathogenic variants in DONSON as a novel cause of Meier-Gorlin syndrome. Journal of medical genetics, 57(3), 195-202. https://doi.org/10.1136/jmedgenet-2019-106396

Chicago Style (17th ed.) Citation

Knapp, Karen M., et al. "Linked-read Genome Sequencing Identifies Biallelic Pathogenic Variants in DONSON as a Novel Cause of Meier-Gorlin Syndrome." Journal of Medical Genetics 57, no. 3 (2020): 195-202. https://doi.org/10.1136/jmedgenet-2019-106396.

MLA (9th ed.) Citation

Knapp, Karen M., et al. "Linked-read Genome Sequencing Identifies Biallelic Pathogenic Variants in DONSON as a Novel Cause of Meier-Gorlin Syndrome." Journal of Medical Genetics, vol. 57, no. 3, 2020, pp. 195-202, https://doi.org/10.1136/jmedgenet-2019-106396.