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

. 2020 Dec ; 4 (6) : e489. [epub] 20201110

Status PubMed-not-MEDLINE Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid33204999
Odkazy

PubMed 33204999
PubMed Central PMC7665249
DOI 10.1097/hs9.0000000000000489
PII: HemaSphere-2020-0193
Knihovny.cz E-zdroje

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