Ülgen, E. Et Al. 2021. Sequential filtering for clinically relevant variants as a method for clinical interpretation of whole exome sequencing findings in glioma. BMC MEDICAL GENOMICS , vol.14, no.1 .

Ülgen, E., Can, Ö., Bilguvar, K., Akyerli Boylu, C., Kılıçturgay Yüksel, Ş., Erşen Danyeli, A., ... Sezerman, O. U.(2021). Sequential filtering for clinically relevant variants as a method for clinical interpretation of whole exome sequencing findings in glioma. BMC MEDICAL GENOMICS , vol.14, no.1.

Ülgen, Ege Et Al. "Sequential filtering for clinically relevant variants as a method for clinical interpretation of whole exome sequencing findings in glioma," BMC MEDICAL GENOMICS , vol.14, no.1, 2021

Ülgen, Ege Et Al. "Sequential filtering for clinically relevant variants as a method for clinical interpretation of whole exome sequencing findings in glioma." BMC MEDICAL GENOMICS , vol.14, no.1, 2021

Ülgen, E. Et Al. (2021) . "Sequential filtering for clinically relevant variants as a method for clinical interpretation of whole exome sequencing findings in glioma." BMC MEDICAL GENOMICS , vol.14, no.1.

@article{article, author={Ege Ülgen Et Al. }, title={Sequential filtering for clinically relevant variants as a method for clinical interpretation of whole exome sequencing findings in glioma}, journal={BMC MEDICAL GENOMICS}, year=2021}