HLOŽKOVÁ, Michaela, Jana FIGULOVÁ, Veronika NAVRKALOVÁ, Jitka MALČÍKOVÁ, Jana ŠMARDOVÁ, Nikola TOM, Yvona BRYCHTOVÁ, Michael DOUBEK, Jiří MAYER, Šárka POSPÍŠILOVÁ and Martin TRBUŠEK. Mutations in SF3B1 gene are selected independently on ATM/TP53 status and reduce the time to first treatment in CLL patients. In Haematologica (2016); 101(s1): 417 (21st Congress of the EHA). 2016. |
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@proceedings{1363946, author = {Hložková, Michaela and Figulová, Jana and Navrkalová, Veronika and Malčíková, Jitka and Šmardová, Jana and Tom, Nikola and Brychtová, Yvona and Doubek, Michael and Mayer, Jiří and Pospíšilová, Šárka and Trbušek, Martin}, booktitle = {Haematologica (2016); 101(s1): 417 (21st Congress of the EHA)}, title = {Mutations in SF3B1 gene are selected independently on ATM/TP53 status and reduce the time to first treatment in CLL patients.}, year = {2016} }
TY - CONF ID - 1363946 AU - Hložková, Michaela - Figulová, Jana - Navrkalová, Veronika - Malčíková, Jitka - Šmardová, Jana - Tom, Nikola - Brychtová, Yvona - Doubek, Michael - Mayer, Jiří - Pospíšilová, Šárka - Trbušek, Martin PY - 2016 TI - Mutations in SF3B1 gene are selected independently on ATM/TP53 status and reduce the time to first treatment in CLL patients. ER -
HLOŽKOVÁ, Michaela, Jana FIGULOVÁ, Veronika NAVRKALOVÁ, Jitka MALČÍKOVÁ, Jana ŠMARDOVÁ, Nikola TOM, Yvona BRYCHTOVÁ, Michael DOUBEK, Jiří MAYER, Šárka POSPÍŠILOVÁ and Martin TRBUŠEK. Mutations in SF3B1 gene are selected independently on ATM/TP53 status and reduce the time to first treatment in CLL patients. In \textit{Haematologica (2016); 101(s1): 417 (21st Congress of the EHA)}. 2016.
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