ERGÜN, M. A. Et Al. 2017. Whole exome sequencing reveals a mutation in an osteogenesis imperfecta patient. META GENE , vol.11 , 137-140.

ERGÜN, M. A., Bilgili, G., Hamurcu, U., & Ertan, A., (2017). Whole exome sequencing reveals a mutation in an osteogenesis imperfecta patient. META GENE , vol.11, 137-140.

ERGÜN, MEHMET Et Al. "Whole exome sequencing reveals a mutation in an osteogenesis imperfecta patient," META GENE , vol.11, 137-140, 2017

ERGÜN, MEHMET A. Et Al. "Whole exome sequencing reveals a mutation in an osteogenesis imperfecta patient." META GENE , vol.11, pp.137-140, 2017

ERGÜN, M. A. Et Al. (2017) . "Whole exome sequencing reveals a mutation in an osteogenesis imperfecta patient." META GENE , vol.11, pp.137-140.

@article{article, author={MEHMET ALİ ERGÜN Et Al. }, title={Whole exome sequencing reveals a mutation in an osteogenesis imperfecta patient}, journal={META GENE}, year=2017, pages={137-140} }