APA aipamena

Nikkhah, E., Safaralizadeh, R., Mohammadiasl, J., Tahmasebi Birgani, M., Hosseinpour Feizi, M. A., & Golchin, N. (2018). Identification of A Novel Compound Heterozygous Mutation in BBS12 in An Iranian Family with Bardet-Biedl Syndrome Using Targeted Next Generation Sequencing. Cell J.

Chicago Style aipamena

Nikkhah, Emad, Reza Safaralizadeh, Javad Mohammadiasl, Maryam Tahmasebi Birgani, Mohammad Ali Hosseinpour Feizi, and Neda Golchin. "Identification of A Novel Compound Heterozygous Mutation In BBS12 in An Iranian Family With Bardet-Biedl Syndrome Using Targeted Next Generation Sequencing." Cell J 2018.

MLA aipamena

Nikkhah, Emad, et al. "Identification of A Novel Compound Heterozygous Mutation In BBS12 in An Iranian Family With Bardet-Biedl Syndrome Using Targeted Next Generation Sequencing." Cell J 2018.