Karakaş, Z. 2024. Identification of the molecular etiology in rare congenital hemolytic anemias using next generation sequencing with exome-based copy number variant analysis. EUROPEAN JOURNAL OF HAEMATOLOGY , vol.3, no.1 , 256-279.

Karakaş, Z., (2024). Identification of the molecular etiology in rare congenital hemolytic anemias using next generation sequencing with exome-based copy number variant analysis. EUROPEAN JOURNAL OF HAEMATOLOGY , vol.3, no.1, 256-279.

Karakaş, Zeynep. "Identification of the molecular etiology in rare congenital hemolytic anemias using next generation sequencing with exome-based copy number variant analysis," EUROPEAN JOURNAL OF HAEMATOLOGY , vol.3, no.1, 256-279, 2024

Karakaş, Zeynep. "Identification of the molecular etiology in rare congenital hemolytic anemias using next generation sequencing with exome-based copy number variant analysis." EUROPEAN JOURNAL OF HAEMATOLOGY , vol.3, no.1, pp.256-279, 2024

Karakaş, Z. (2024) . "Identification of the molecular etiology in rare congenital hemolytic anemias using next generation sequencing with exome-based copy number variant analysis." EUROPEAN JOURNAL OF HAEMATOLOGY , vol.3, no.1, pp.256-279.

@article{article, author={Zeynep KARAKAŞ}, title={Identification of the molecular etiology in rare congenital hemolytic anemias using next generation sequencing with exome-based copy number variant analysis}, journal={EUROPEAN JOURNAL OF HAEMATOLOGY}, year=2024, pages={256-279} }