Altındirek, D. Et Al. 2023. Characterization of Hereditary Hemolytic Anemia cases in Turkey by Whole Exome Sequencing . EHA-SWG Scientific Meeting on Red Cell and Iron Metabolism Defects: From Basic Science to Clinical Case Application , (Budapest, Hungary).

Altındirek, D., Tuğcu, D., Karaman, S., Erbilgin, Y., Sayitoğlu, M., & Karakaş, Z., (2023). Characterization of Hereditary Hemolytic Anemia cases in Turkey by Whole Exome Sequencing . EHA-SWG Scientific Meeting on Red Cell and Iron Metabolism Defects: From Basic Science to Clinical Case Application, Budapest, Hungary

Altındirek, Didem Et Al. "Characterization of Hereditary Hemolytic Anemia cases in Turkey by Whole Exome Sequencing ," EHA-SWG Scientific Meeting on Red Cell and Iron Metabolism Defects: From Basic Science to Clinical Case Application, Budapest, Hungary, 2023

Altındirek, Didem Et Al. "Characterization of Hereditary Hemolytic Anemia cases in Turkey by Whole Exome Sequencing ." EHA-SWG Scientific Meeting on Red Cell and Iron Metabolism Defects: From Basic Science to Clinical Case Application , Budapest, Hungary, 2023

Altındirek, D. Et Al. (2023) . "Characterization of Hereditary Hemolytic Anemia cases in Turkey by Whole Exome Sequencing ." EHA-SWG Scientific Meeting on Red Cell and Iron Metabolism Defects: From Basic Science to Clinical Case Application , Budapest, Hungary.

@conferencepaper{conferencepaper, author={Didem ALTINDİREK Et Al. }, title={Characterization of Hereditary Hemolytic Anemia cases in Turkey by Whole Exome Sequencing }, congress name={EHA-SWG Scientific Meeting on Red Cell and Iron Metabolism Defects: From Basic Science to Clinical Case Application}, city={Budapest}, country={Hungary}, year={2023}}