ERGÜN, M. A. Et Al. 2016. Whole Exome Sequencing reveals a mutation in an osteogenesis imperfecta patient. European Society of Human Genetics 2016 .

ERGÜN, M. A., bilgili, g., hamurcu, u., & ERTAN, A. A., (2016). Whole Exome Sequencing reveals a mutation in an osteogenesis imperfecta patient . European Society of Human Genetics 2016

ERGÜN, MEHMET Et Al. "Whole Exome Sequencing reveals a mutation in an osteogenesis imperfecta patient," European Society of Human Genetics 2016, 2016

ERGÜN, MEHMET A. Et Al. "Whole Exome Sequencing reveals a mutation in an osteogenesis imperfecta patient." European Society of Human Genetics 2016 , 2016

ERGÜN, M. A. Et Al. (2016) . "Whole Exome Sequencing reveals a mutation in an osteogenesis imperfecta patient." European Society of Human Genetics 2016 .

@conferencepaper{conferencepaper, author={MEHMET ALİ ERGÜN Et Al. }, title={Whole Exome Sequencing reveals a mutation in an osteogenesis imperfecta patient}, congress name={European Society of Human Genetics 2016}, city={}, country={}, year={2016}}