IŞIK, E. Et Al. 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.113, no.1 , 82-89.

IŞIK, E., AYDINOK, Y., Albayrak, C., Durmus, B., Karakas, Z., Orhan, M. F., ... SARPER, N.(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.113, no.1, 82-89.

IŞIK, ESRA Et Al. "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.113, no.1, 82-89, 2024

IŞIK, ESRA Et Al. "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.113, no.1, pp.82-89, 2024

IŞIK, E. Et Al. (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.113, no.1, pp.82-89.

@article{article, author={ESRA IŞIK Et Al. }, 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={82-89} }