APA Alıntı

Vona, B., Hofrichter, M., Neuner, C., Schröder, J., Gehrig, A., Hennermann, J., . . . Haaf, T. (2015). DFNB16 is a frequent cause of congenital hearing impairment: Implementation of STRC mutation analysis in routine diagnostics. Clin Genet.

Chicago Stili Alıntı

Vona, B., et al. "DFNB16 Is a Frequent Cause of Congenital Hearing Impairment: Implementation of STRC Mutation Analysis in Routine Diagnostics." Clin Genet 2015.

MLA Alıntı

Vona, B., et al. "DFNB16 Is a Frequent Cause of Congenital Hearing Impairment: Implementation of STRC Mutation Analysis in Routine Diagnostics." Clin Genet 2015.