MENGEN, E. Et Al. 2018. A Novel Frameshift Mutation in ESCO2 Gene in Roberts Syndrome.. Journal of the College of Physicians and Surgeons--Pakistan : JCPSP , vol.28 , 403-405.

MENGEN, E., Kotan, L. D., UCAKTURK, S., TOPALOĞLU, A. K., & YÜKSEL, B., (2018). A Novel Frameshift Mutation in ESCO2 Gene in Roberts Syndrome.. Journal of the College of Physicians and Surgeons--Pakistan : JCPSP , vol.28, 403-405.

MENGEN, E Et Al. "A Novel Frameshift Mutation in ESCO2 Gene in Roberts Syndrome.," Journal of the College of Physicians and Surgeons--Pakistan : JCPSP , vol.28, 403-405, 2018

MENGEN, E Et Al. "A Novel Frameshift Mutation in ESCO2 Gene in Roberts Syndrome.." Journal of the College of Physicians and Surgeons--Pakistan : JCPSP , vol.28, pp.403-405, 2018

MENGEN, E. Et Al. (2018) . "A Novel Frameshift Mutation in ESCO2 Gene in Roberts Syndrome.." Journal of the College of Physicians and Surgeons--Pakistan : JCPSP , vol.28, pp.403-405.

@article{article, author={E MENGEN Et Al. }, title={A Novel Frameshift Mutation in ESCO2 Gene in Roberts Syndrome.}, journal={Journal of the College of Physicians and Surgeons--Pakistan : JCPSP}, year=2018, pages={403-405} }