Şeker-Yılmaz, B. Et Al. 2019. Short-chainacyl-CoA dehydrogenase deficiency: two siblings with two distinct phenotypes. Annual Symposium of the Society for the Study of Inborn Errors of Metabolism, Rotterdam, The Netherlands .

Şeker-Yılmaz, B., KILAVUZ, S., KOR, D., BULUT, F. D., YILDIZDAŞ, R. D., TOLUNAY, İ., ... ÖNENLİ MUNGAN, H. N.(2019). Short-chainacyl-CoA dehydrogenase deficiency: two siblings with two distinct phenotypes . Annual Symposium of the Society for the Study of Inborn Errors of Metabolism, Rotterdam, The Netherlands

Şeker-Yılmaz, Berna Et Al. "Short-chainacyl-CoA dehydrogenase deficiency: two siblings with two distinct phenotypes," Annual Symposium of the Society for the Study of Inborn Errors of Metabolism, Rotterdam, The Netherlands, 2019

Şeker-Yılmaz, Berna Et Al. "Short-chainacyl-CoA dehydrogenase deficiency: two siblings with two distinct phenotypes." Annual Symposium of the Society for the Study of Inborn Errors of Metabolism, Rotterdam, The Netherlands , 2019

Şeker-Yılmaz, B. Et Al. (2019) . "Short-chainacyl-CoA dehydrogenase deficiency: two siblings with two distinct phenotypes." Annual Symposium of the Society for the Study of Inborn Errors of Metabolism, Rotterdam, The Netherlands .

@conferencepaper{conferencepaper, author={Berna Şeker-Yılmaz Et Al. }, title={Short-chainacyl-CoA dehydrogenase deficiency: two siblings with two distinct phenotypes}, congress name={Annual Symposium of the Society for the Study of Inborn Errors of Metabolism, Rotterdam, The Netherlands}, city={}, country={}, year={2019}}