Dyfyniad APA

Mansour-Hendili, L., Aissat, A., Badaoui, B., Sakka, M., Gameiro, C., Ortonne, V., . . . Galactéros, F. (2020). Exome sequencing for diagnosis of congenital hemolytic anemia. Orphanet J Rare Dis.

Dyfyniad Arddull Chicago

Mansour-Hendili, Lamisse, et al. "Exome Sequencing for Diagnosis of Congenital Hemolytic Anemia." Orphanet J Rare Dis 2020.

Dyfyniad MLA

Mansour-Hendili, Lamisse, et al. "Exome Sequencing for Diagnosis of Congenital Hemolytic Anemia." Orphanet J Rare Dis 2020.

Rhybudd: Mae'n bosib nad yw'r dyfyniadau hyn bob amser yn 100% cywir.