학술논문
Identification of the molecular etiology in rare congenital hemolytic anemias using next-generation sequencing with exome-based copy number variant analysis
Document Type
Article
Author
Isik, E.; Durmus, B.; Karadas, N.; Cogulu, O.; Ozkinay, F.; Atik, T.; Aydinok, Y.; Albayrak, C.; Karakas, Z.; Tugcu, D.; Karaman, S.; Unuvar, A.; Bilici, M.; Orhan, M.F.; Sarper, N.; Gelen, S.A.; Zengin, E.; Aydın, S.; Unal, S.; Oymak, Y.; Turedi, A.; Albayrak, D.; Tayfun, F.; Tobu, M.; Unal, E.; Ozcan, A.; Unal, S.; Aksu, T.; Azik, F.; Ay, Y.; Albudak, E.; Eker, I.; Karakaya, T.
Source
In: European Journal of Haematology . (European Journal of Haematology, July 2024, 113(1):82-89)
Subject
Language
English
ISSN
16000609
09024441
09024441