Gedikbaşı, A. Et Al. 2021. Diagnosis utility of Whole Exome Sequencing in patients with suspected mitochondrial disease:the single center experience in Turkish population.. XIV International Congress of Inborn Errors of Metabolism , (Sydney, Australia), 227-228.

Gedikbaşı, A., Toksoy, G., Karaca, M., Balcı, M. C., Güleç, Ç., Selamioğlu, A., ... Güneş, S.(2021). Diagnosis utility of Whole Exome Sequencing in patients with suspected mitochondrial disease:the single center experience in Turkish population. . XIV International Congress of Inborn Errors of Metabolism (pp.227-228). Sydney, Australia

Gedikbaşı, Asuman Et Al. "Diagnosis utility of Whole Exome Sequencing in patients with suspected mitochondrial disease:the single center experience in Turkish population.," XIV International Congress of Inborn Errors of Metabolism, Sydney, Australia, 2021

Gedikbaşı, Asuman Et Al. "Diagnosis utility of Whole Exome Sequencing in patients with suspected mitochondrial disease:the single center experience in Turkish population.." XIV International Congress of Inborn Errors of Metabolism , Sydney, Australia, pp.227-228, 2021

Gedikbaşı, A. Et Al. (2021) . "Diagnosis utility of Whole Exome Sequencing in patients with suspected mitochondrial disease:the single center experience in Turkish population.." XIV International Congress of Inborn Errors of Metabolism , Sydney, Australia, pp.227-228.

@conferencepaper{conferencepaper, author={Asuman GEDİKBAŞI Et Al. }, title={Diagnosis utility of Whole Exome Sequencing in patients with suspected mitochondrial disease:the single center experience in Turkish population.}, congress name={XIV International Congress of Inborn Errors of Metabolism}, city={Sydney}, country={Australia}, year={2021}, pages={227-228} }