Esin Kantekin

A novel KIF11 mutation in a Turkish patient with microcephaly, lymphedema, and chorioretinal dysplasia from a consanguineous family

S. Jeffery, F. Hazan, F. Ozkinay, 2012, American journal of medical genetics. Part A.

FATCO syndrome: a new case and review of the literature

F. Hazan, Nagehan Katipoğlu, Ş. Çalkavur, 2016 .