Identification of Fusion Gene Breakpoints is Feasible and Facilitates Accurate Sensitive Minimal Residual Disease Monitoring on Genomic Level in Patients With PML-RARA, CBFB-MYH11, and RUNX1-RUNX1T1

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書目詳細資料
發表在:Hemasphere
Main Authors: Lukes, Julius, Winkowska, Lucie, Zwyrtkova, Martina, Starkova, Julia, Sramkova, Lucie, Stary, Jan, Trka, Jan, Zuna, Jan, Zaliova, Marketa
格式: Artigo
語言:Inglês
出版: Lippincott Williams & Wilkins 2020
主題:
Letter
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC7665249/
https://ncbi.nlm.nih.gov/pubmed/33204999
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/HS9.0000000000000489
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