APA (7th ed.) Citation

Debladis, J., Valette, M., Strenilkov, K., Mantoulan, C., Thuilleaux, D., Laurier, V., . . . Tauber, M. (2019). Face processing and exploration of social signals in Prader-Willi syndrome: A genetic signature. Orphanet Journal of Rare Diseases, 14(1), 1. https://doi.org/10.1186/s13023-019-1221-3

Chicago Style (17th ed.) Citation

Debladis, Jimmy, Marion Valette, Kuzma Strenilkov, Carine Mantoulan, Denise Thuilleaux, Virginie Laurier, Catherine Molinas, Pascal Barone, and Maïthé Tauber. "Face Processing and Exploration of Social Signals in Prader-Willi Syndrome: A Genetic Signature." Orphanet Journal of Rare Diseases 14, no. 1 (2019): 1. https://doi.org/10.1186/s13023-019-1221-3.

MLA (9th ed.) Citation

Debladis, Jimmy, et al. "Face Processing and Exploration of Social Signals in Prader-Willi Syndrome: A Genetic Signature." Orphanet Journal of Rare Diseases, vol. 14, no. 1, 2019, p. 1, https://doi.org/10.1186/s13023-019-1221-3.