G. Sahin

ANOVELWT1GENEMUTATIONINANEWBORNINFANT DIAGNOSEDWITHDENYS-DRASHSYNDROME

Z. Aycan, F. Ozaltin, A. Zenciroğlu, 2012 .

A novel WT1 gene mutation in a newborn infant diagnosed with Denys-Drash syndrome.

Z. Aycan, F. Ozaltin, A. Zenciroğlu, 2012, Genetic counseling.

Burkholderia cepacia as a Cause of Ecthyma Gangrenosum-like Lesion

G. Aygencel, M. Dizbay, G. Sahin, 2008, Infection.