A Novel Frameshift Mutation in ESCO2 Gene in Roberts Syndrome


MENGEN E., KOTAN L. D., Uçaktürk S. A., TOPALOĞLU A. K., YÜKSEL B.

JCPSP-JOURNAL OF THE COLLEGE OF PHYSICIANS AND SURGEONS PAKISTAN, cilt.5, ss.403-405, 2018 (SCI-Expanded)