- Molecular Analysis of Chromosome 21 in a Patient With a Phenotype of Down Syndrome and Apparently Normal Karyotype1996 | Second Faculty of Medicine
- Chromophobe renal cell carcinoma with prominent lymph node metastasis and polysomy of chromosome 21: poorly differentiated form or2011 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- A 15 Mb large paracentric chromosome 21 inversion identified in Czech population through a pair of flanking duplications2014 | Second Faculty of Medicine
- Extracellular chromosome 21 - derived microRNAs in maternal circulation: evaluation of their diagnostic potential for screening of Down syndrome2012 | First Faculty of Medicine, Third Faculty of Medicine
- Chromosome 21 gain is dispensable for transient myeloproliferative disorder driven by a novel GATA1 mutation2020 | Second Faculty of Medicine
- Importance of Down syndrome in haematology2022 | Second Faculty of Medicine, Central Library of Charles University
- Analysis of SYNJI, a candidate gene for 21q22 linked bipolar disorder. A replication study2004 | First Faculty of Medicine
- Extracellular chromosome 21-derived microRNAs in euploid & aneuploid pregnancies2013 | First Faculty of Medicine, Third Faculty of Medicine
- PAPP-A/proMBP complex in prenatal screening of severe fetal disorders and postnatal detection of acute coronary disease2004 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Intragenic amplification of PAX5: a novel subgroup in B-cell precursor acute lymphoblastic leukemia?2017 | Second Faculty of Medicine
- Novel insights into the mixed germ cell-sex cord stromal tumor of the testis: detection of chromosomal aneuploidy and further morphological evidence supporting the neoplastic nature of the germ cell component2020 | Faculty of Medicine in Pilsen
- Differentially expressed miRNAs in trisomy 21 placentas2016 | First Faculty of Medicine
- Rapid non-invasive prenatal screening test for trisomy 21 based on digital droplet PCR2023 | First Faculty of Medicine
- Hsa-mir-125b-2 is highly expressed in childhood ETV6/RUNX1 (TEL/AML1) leukemias and confers survival advantage to growth inhibitory signals independent of p532010 | Second Faculty of Medicine
- Digital polymerase chain reaction duplexing method in a single fluorescence channel2023 | First Faculty of Medicine
- Maternal plasma DNA testing for aneuploidy in pregnancies achieved by assisted reproductive technologies2014 | Central Library of Charles University
- Physiological and pathological functions of beta-amyloid in the brain and alzheimer's disease: A review2020 | First Faculty of Medicine
- Clinical Course in 22 Children and Adultsfrom Central and Eastern Europe2002 | Third Faculty of Medicine
- Determination of Advantages and Limitations of qPCR Duplexing in a Single Fluorescent Channel2021 | First Faculty of Medicine
- Chromophobe renal cell carcinoma - chromosomal aberration variability and its relation to Paner grading system: an array CGH and FISH analysis of 37 cases2013 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- The Reduced Use of Invasive Procedures Leads to a Change of Frequencies of Prenatally Detected Chromosomal Aberrations: Population Data From the Years 2012-20162023 | First Faculty of Medicine, Third Faculty of Medicine, Central Library of Charles University
