Kılavuz, S. Et Al. 2023. Evaluation of Patients Diagnosed with Congenital Glycosylation Defects: A Rainbow of Inherited Metabolic Disorders. Çocuk Dergisi , vol.23 , 31-40.

Kılavuz, S., Bulut, F. D., Kor, D., Şeker Yılmaz, B., Bişgin, A., Demir, F., ... Atmış, B.(2023). Evaluation of Patients Diagnosed with Congenital Glycosylation Defects: A Rainbow of Inherited Metabolic Disorders. Çocuk Dergisi , vol.23, 31-40.

Kılavuz, Sebile Et Al. "Evaluation of Patients Diagnosed with Congenital Glycosylation Defects: A Rainbow of Inherited Metabolic Disorders," Çocuk Dergisi , vol.23, 31-40, 2023

Kılavuz, Sebile Et Al. "Evaluation of Patients Diagnosed with Congenital Glycosylation Defects: A Rainbow of Inherited Metabolic Disorders." Çocuk Dergisi , vol.23, pp.31-40, 2023

Kılavuz, S. Et Al. (2023) . "Evaluation of Patients Diagnosed with Congenital Glycosylation Defects: A Rainbow of Inherited Metabolic Disorders." Çocuk Dergisi , vol.23, pp.31-40.

@article{article, author={Sebile Kılavuz Et Al. }, title={Evaluation of Patients Diagnosed with Congenital Glycosylation Defects: A Rainbow of Inherited Metabolic Disorders}, journal={Çocuk Dergisi}, year=2023, pages={31-40} }