A Novel Frameshift Mutation in ESCO2 Gene in Roberts Syndrome.


MENGEN E., Kotan L. D., UCAKTURK S., TOPALOĞLU A. K., YÜKSEL B.

Journal of the College of Physicians and Surgeons--Pakistan : JCPSP, cilt.28, ss.403-405, 2018 (SCI-Expanded) identifier identifier identifier