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-Zitierstil (17. Ausg.)Rahmani, E. S., H. Azarpara, M. F. Abazari, M. R. Mohajeri, M. Nasimi, R. Ghorbani, A. Azizpour, und 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-Zitierstil (8. Ausg.)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.