Güneş, D. Et Al. 2019. Isobutyryl-coA dehydrogenase deficiency: a rare disease detectable by tandem mass spectrometry. International Inborn Errors of Metabolism and Nutrition Congress. , (İstanbul, Turkey), 535-536.

Güneş, D., İşeri Küskü, Z. A., Güneş, S., Balcı, M. C., Demirkol, M., & Gökçay, G. F., (2019). Isobutyryl-coA dehydrogenase deficiency: a rare disease detectable by tandem mass spectrometry . International Inborn Errors of Metabolism and Nutrition Congress. (pp.535-536). İstanbul, Turkey

Güneş, Dilek Et Al. "Isobutyryl-coA dehydrogenase deficiency: a rare disease detectable by tandem mass spectrometry," International Inborn Errors of Metabolism and Nutrition Congress. , İstanbul, Turkey, 2019

Güneş, Dilek Et Al. "Isobutyryl-coA dehydrogenase deficiency: a rare disease detectable by tandem mass spectrometry." International Inborn Errors of Metabolism and Nutrition Congress. , İstanbul, Turkey, pp.535-536, 2019

Güneş, D. Et Al. (2019) . "Isobutyryl-coA dehydrogenase deficiency: a rare disease detectable by tandem mass spectrometry." International Inborn Errors of Metabolism and Nutrition Congress. , İstanbul, Turkey, pp.535-536.

@conferencepaper{conferencepaper, author={Dilek GÜNEŞ Et Al. }, title={Isobutyryl-coA dehydrogenase deficiency: a rare disease detectable by tandem mass spectrometry}, congress name={International Inborn Errors of Metabolism and Nutrition Congress. }, city={İstanbul}, country={Turkey}, year={2019}, pages={535-536} }