S. CİNGÖZ Et Al. , "A novel missense mutation (N78D) in a family with von Hippel-Lindau disease with central nervous system haemangioblastomas, pancreatic and renal cysts," FAMILIAL CANCER , vol.12, no.1, pp.111-117, 2013
CİNGÖZ, S. Et Al. 2013. A novel missense mutation (N78D) in a family with von Hippel-Lindau disease with central nervous system haemangioblastomas, pancreatic and renal cysts. FAMILIAL CANCER , vol.12, no.1 , 111-117.
CİNGÖZ, S., van der Luijt, R. B., Kurt, E., Apaydin, M., Akkol, I., & Ozgen, M. H., (2013). A novel missense mutation (N78D) in a family with von Hippel-Lindau disease with central nervous system haemangioblastomas, pancreatic and renal cysts. FAMILIAL CANCER , vol.12, no.1, 111-117.
CİNGÖZ, SULTAN Et Al. "A novel missense mutation (N78D) in a family with von Hippel-Lindau disease with central nervous system haemangioblastomas, pancreatic and renal cysts," FAMILIAL CANCER , vol.12, no.1, 111-117, 2013
CİNGÖZ, SULTAN Et Al. "A novel missense mutation (N78D) in a family with von Hippel-Lindau disease with central nervous system haemangioblastomas, pancreatic and renal cysts." FAMILIAL CANCER , vol.12, no.1, pp.111-117, 2013
CİNGÖZ, S. Et Al. (2013) . "A novel missense mutation (N78D) in a family with von Hippel-Lindau disease with central nervous system haemangioblastomas, pancreatic and renal cysts." FAMILIAL CANCER , vol.12, no.1, pp.111-117.
@article{article, author={SULTAN CİNGÖZ Et Al. }, title={A novel missense mutation (N78D) in a family with von Hippel-Lindau disease with central nervous system haemangioblastomas, pancreatic and renal cysts}, journal={FAMILIAL CANCER}, year=2013, pages={111-117} }