MENGEN, E. Et Al. 2018. A Novel Frameshift Mutation in ESCO2 Gene in Roberts Syndrome. JCPSP-JOURNAL OF THE COLLEGE OF PHYSICIANS AND SURGEONS PAKISTAN , vol.5 , 403-405.

MENGEN, E., KOTAN, L. D., Uçaktürk, S. A., TOPALOĞLU, A. K., & YÜKSEL, B., (2018). A Novel Frameshift Mutation in ESCO2 Gene in Roberts Syndrome. JCPSP-JOURNAL OF THE COLLEGE OF PHYSICIANS AND SURGEONS PAKISTAN , vol.5, 403-405.

MENGEN, E Et Al. "A Novel Frameshift Mutation in ESCO2 Gene in Roberts Syndrome," JCPSP-JOURNAL OF THE COLLEGE OF PHYSICIANS AND SURGEONS PAKISTAN , vol.5, 403-405, 2018

MENGEN, E Et Al. "A Novel Frameshift Mutation in ESCO2 Gene in Roberts Syndrome." JCPSP-JOURNAL OF THE COLLEGE OF PHYSICIANS AND SURGEONS PAKISTAN , vol.5, pp.403-405, 2018

MENGEN, E. Et Al. (2018) . "A Novel Frameshift Mutation in ESCO2 Gene in Roberts Syndrome." JCPSP-JOURNAL OF THE COLLEGE OF PHYSICIANS AND SURGEONS PAKISTAN , vol.5, pp.403-405.

@article{article, author={E MENGEN Et Al. }, title={A Novel Frameshift Mutation in ESCO2 Gene in Roberts Syndrome}, journal={JCPSP-JOURNAL OF THE COLLEGE OF PHYSICIANS AND SURGEONS PAKISTAN}, year=2018, pages={403-405} }