B. Katrincsáková

Detection of His1069Gln mutation in Wilson disease by bidirectional PCR amplification of specific alleles (BI-PASA) test.

L. Kádasi, G. Minárik, M. Baldovič, 2007, General physiology and biophysics.

The role of new technologies in myeloproliferative neoplasms: Application of next‐generation sequencing in myelofibrosis

K. Indrák, J. Navrátilová, T. Papajík, 2021, International journal of laboratory hematology.

Identification of e6a2 BCR-ABL fusion in a Philadelphia-positive CML with marked basophilia: implications for treatment strategy.

V. Divoky, Lenka Calabkova, M. Jarošová, 2011, Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia.

Methylation analysis of the imprinted DLK1-GTL2 domain supports the random parental origin of the IGH-involving del(14q) in B-cell malignancies

M. Georges, L. Michaux, M. Jarošová, 2009, Epigenetics.

Comparison of new flu-bu12-tg conditioning with the standard bu-cy myeloablative regimen in patients undergoing allogeneic stem cell transplantation for acute myeloid leukemia.

M. Jarošová, Z. Pikalová, K. Indrák, 2011, Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia.

Prognostic factors and treatment outcome in 1,516 adult patients with de novo and secondary acute myeloid leukemia in 1999-2009 in 5 hematology intensive care centers in the Czech Republic.

T. Pavlík, L. Dušek, K. Michalová, 2010, Neoplasma.

Recurrent breakpoints in 14q32.13/TCL1A region in mature B-cell neoplasms with villous lymphocytes

P. Van Loo, A. Delannoy, C. de Wolf‐Peeters, 2012, Leukemia & lymphoma.