APA Alıntı

Sargolzaeiaval, F., Zhang, J., Schleit, J., Lessel, D., Kubisch, C., Precioso, D. R., . . . Oshima, J. (2018). CTC1 mutations in a Brazilian family with progeroid features and recurrent bone fractures. Mol Genet Genomic Med.

Chicago Stili Alıntı

Sargolzaeiaval, Forough, et al. "CTC1 Mutations in a Brazilian Family With Progeroid Features and Recurrent Bone Fractures." Mol Genet Genomic Med 2018.

MLA Alıntı

Sargolzaeiaval, Forough, et al. "CTC1 Mutations in a Brazilian Family With Progeroid Features and Recurrent Bone Fractures." Mol Genet Genomic Med 2018.