Atay, F. Y. Et Al. 2017. Congenital Glucose–Galactose Malabsorption in a Turkish Newborn: A Novel Mutation of Na+/Glucose Cotransporter Gene. Digestive Diseases and Sciences , vol.62, no.1 , 280-281.

Atay, F. Y., Derme, T., Uras, N., CEYLANER, G., CEYLANER, S., Sari, F. N., ... Oguz, S. S.(2017). Congenital Glucose–Galactose Malabsorption in a Turkish Newborn: A Novel Mutation of Na+/Glucose Cotransporter Gene. Digestive Diseases and Sciences , vol.62, no.1, 280-281.

Atay, Funda Et Al. "Congenital Glucose–Galactose Malabsorption in a Turkish Newborn: A Novel Mutation of Na+/Glucose Cotransporter Gene," Digestive Diseases and Sciences , vol.62, no.1, 280-281, 2017

Atay, Funda Y. Et Al. "Congenital Glucose–Galactose Malabsorption in a Turkish Newborn: A Novel Mutation of Na+/Glucose Cotransporter Gene." Digestive Diseases and Sciences , vol.62, no.1, pp.280-281, 2017

Atay, F. Y. Et Al. (2017) . "Congenital Glucose–Galactose Malabsorption in a Turkish Newborn: A Novel Mutation of Na+/Glucose Cotransporter Gene." Digestive Diseases and Sciences , vol.62, no.1, pp.280-281.

@article{article, author={Funda Yavanoglu Atay Et Al. }, title={Congenital Glucose–Galactose Malabsorption in a Turkish Newborn: A Novel Mutation of Na+/Glucose Cotransporter Gene}, journal={Digestive Diseases and Sciences}, year=2017, pages={280-281} }