KOTAŠKOVÁ, Jana, Andrea MAREČKOVÁ, Daniela POKRIVČÁKOVÁ, Eva ONDROUŠKOVÁ, Anna FIDRICHOVÁ, Lenka BRYJOVÁ, Viera HRABČÁKOVÁ, Jakub Paweł PORC, Veronika NAVRKALOVÁ, Karla PLEVOVÁ, Marie JAROŠOVÁ, Šárka POSPÍŠILOVÁ, Martin ŠTORK and Luděk POUR. Identification of genetic aberrations in multiple myeloma patients with low tumour burden using comprehensive NGS testing. In EHA-SWG Scientific Meeting Integrated Cell Tracking in Oncohematology: Diagnosis, Targeted Therapy and Residual Disease, Francie, Bordeaux. 2022.
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Basic information
Original name Identification of genetic aberrations in multiple myeloma patients with low tumour burden using comprehensive NGS testing.
Authors KOTAŠKOVÁ, Jana, Andrea MAREČKOVÁ, Daniela POKRIVČÁKOVÁ, Eva ONDROUŠKOVÁ, Anna FIDRICHOVÁ, Lenka BRYJOVÁ, Viera HRABČÁKOVÁ, Jakub Paweł PORC, Veronika NAVRKALOVÁ, Karla PLEVOVÁ, Marie JAROŠOVÁ, Šárka POSPÍŠILOVÁ, Martin ŠTORK and Luděk POUR.
Edition EHA-SWG Scientific Meeting Integrated Cell Tracking in Oncohematology: Diagnosis, Targeted Therapy and Residual Disease, Francie, Bordeaux, 2022.
Other information
Type of outcome Conference abstract
Confidentiality degree is not subject to a state or trade secret
Organization unit Central European Institute of Technology
Changed by Changed by: Bc. Kateřina Kolesová, učo 112275. Changed: 9/12/2022 15:16.
Links
NV19-03-00091, research and development projectName: Komplexní prognostický a prediktivní panel pro pacienty s chronickou lymfocytární leukémií: nástroj sekvenování nové generace vhodný pro klinickou praxi i studium genetického pozadí průběhu choroby
Investor: Ministry of Health of the CR
PrintDisplayed: 28/7/2024 01:26