APA (7th ed.) Citation

Rahmani, E. S., Azarpara, H., Abazari, M. F., Mohajeri, M. R., Nasimi, M., Ghorbani, R., . . . Rahimi, H. (2020). Novel mutation s.7348C>T in NF1 gene identified by whole¬exome sequencing in patient with overlapping clinical symptoms of neurofibromatosis type 1 and bannayan¬riley¬ruvalcaba syndrome.

Chicago Style (17th ed.) Citation

Rahmani, E. S., H. Azarpara, M. F. Abazari, M. R. Mohajeri, M. Nasimi, R. Ghorbani, A. Azizpour, and H. Rahimi. Novel Mutation S.7348C>T in NF1 Gene Identified by Whole¬exome Sequencing in Patient with Overlapping Clinical Symptoms of Neurofibromatosis Type 1 and Bannayan¬riley¬ruvalcaba Syndrome. 2020.

MLA (8th ed.) Citation

Rahmani, E. S., et al. Novel Mutation S.7348C>T in NF1 Gene Identified by Whole¬exome Sequencing in Patient with Overlapping Clinical Symptoms of Neurofibromatosis Type 1 and Bannayan¬riley¬ruvalcaba Syndrome. 2020.

Warning: These citations may not always be 100% accurate.