Kucukcongar, A. Et Al. 2015. A CASE WITH RARE TYPE OF CONGENITAL DISORDER OF GLYCOSYLATION: PGM1-CDG. GENETIC COUNSELING , vol.26, no.1 , 87-90.

Kucukcongar, A., Tumer, L., EZGÜ, F. S., Kasapkara, C. S., Jaeken, J., Matthijs, G., ... Rymen, D.(2015). A CASE WITH RARE TYPE OF CONGENITAL DISORDER OF GLYCOSYLATION: PGM1-CDG. GENETIC COUNSELING , vol.26, no.1, 87-90.

Kucukcongar, A. Et Al. "A CASE WITH RARE TYPE OF CONGENITAL DISORDER OF GLYCOSYLATION: PGM1-CDG," GENETIC COUNSELING , vol.26, no.1, 87-90, 2015

Kucukcongar, A. Et Al. "A CASE WITH RARE TYPE OF CONGENITAL DISORDER OF GLYCOSYLATION: PGM1-CDG." GENETIC COUNSELING , vol.26, no.1, pp.87-90, 2015

Kucukcongar, A. Et Al. (2015) . "A CASE WITH RARE TYPE OF CONGENITAL DISORDER OF GLYCOSYLATION: PGM1-CDG." GENETIC COUNSELING , vol.26, no.1, pp.87-90.

@article{article, author={A. Kucukcongar Et Al. }, title={A CASE WITH RARE TYPE OF CONGENITAL DISORDER OF GLYCOSYLATION: PGM1-CDG}, journal={GENETIC COUNSELING}, year=2015, pages={87-90} }