Identification of the molecular etiology in rare congenital hemolytic anemias using next-generation sequencing with exome-based copy number variant analysis.
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Isik E, et al.
Eur J Haematol. 2024 Mar 31. doi: 10.1111/ejh.14194. Online ahead of print.
Eur J Haematol. 2024.
PMID: 38556258