E. IŞIK 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 , 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 .
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 .
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 , 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 , 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 .
@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}