APA Alıntı

Rejeb, I., Jilani, H., Elaribi, Y., Hizem, S., Hila, L., Zillahrdt, J. L., . . . Benjemaa, L. (2017). First case report of Cohen syndrome in the Tunisian population caused by VPS13B mutations. BMC Med Genet.

Chicago Stili Alıntı

Rejeb, Imen, Houweyda Jilani, Yasmina Elaribi, Syrine Hizem, Lamia Hila, Julia Lauer Zillahrdt, Jamel Chelly, ve Lamia Benjemaa. "First Case Report of Cohen Syndrome in the Tunisian Population Caused By VPS13B Mutations." BMC Med Genet 2017.

MLA Alıntı

Rejeb, Imen, et al. "First Case Report of Cohen Syndrome in the Tunisian Population Caused By VPS13B Mutations." BMC Med Genet 2017.