TÜMER, L. Et Al. 2015. Cobalamin C disease with hypopigmented cutaneousfindings A unique case. annual symposium of the society for the study of inborn errors of metabolism , (Lyon, France), 319.

TÜMER, L., ARHAN, E., OKUR, İ., Aydın, K., Hirfanoğlu, T., Karaoğlu, A., ... Öztürk, Z.(2015). Cobalamin C disease with hypopigmented cutaneousfindings A unique case . annual symposium of the society for the study of inborn errors of metabolism (pp.319). Lyon, France

TÜMER, LEYLA Et Al. "Cobalamin C disease with hypopigmented cutaneousfindings A unique case," annual symposium of the society for the study of inborn errors of metabolism, Lyon, France, 2015

TÜMER, LEYLA Et Al. "Cobalamin C disease with hypopigmented cutaneousfindings A unique case." annual symposium of the society for the study of inborn errors of metabolism , Lyon, France, pp.319, 2015

TÜMER, L. Et Al. (2015) . "Cobalamin C disease with hypopigmented cutaneousfindings A unique case." annual symposium of the society for the study of inborn errors of metabolism , Lyon, France, p.319.

@conferencepaper{conferencepaper, author={LEYLA TÜMER Et Al. }, title={Cobalamin C disease with hypopigmented cutaneousfindings A unique case}, congress name={annual symposium of the society for the study of inborn errors of metabolism}, city={Lyon}, country={France}, year={2015}, pages={319} }