APA Alıntı

Rush, E. T., Caldwell, K. S., Kreikemeier, R. M., Lutz, R. E., & Esposito, P. W. (2014). Osteogenesis imperfecta caused by PPIB mutation with severe phenotype and congenital hearing loss. J Pediatr Genet.

Chicago Stili Alıntı

Rush, Eric T., Kathleen S. Caldwell, Rose M. Kreikemeier, Richard E. Lutz, ve Paul W. Esposito. "Osteogenesis Imperfecta Caused By PPIB Mutation With Severe Phenotype and Congenital Hearing Loss." J Pediatr Genet 2014.

MLA Alıntı

Rush, Eric T., et al. "Osteogenesis Imperfecta Caused By PPIB Mutation With Severe Phenotype and Congenital Hearing Loss." J Pediatr Genet 2014.