- Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism1998 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Trisomy X syndrome with dystonia and a pathogenic SATB1 variant2021 | First Faculty of Medicine
- Left ventricle shortening fraction: a comparison between euploid and trisomy 21 fetuses in the first trimester2010 | Publication without faculty affiliation
- Lethal syndromes in pediatrics – three cases of trisomy 182023 | Publication without faculty affiliation
- Rapid non-invasive prenatal screening test for trisomy 21 based on digital droplet PCR2023 | First Faculty of Medicine
- Are we justified to classify patients with two unrelated clones with del(5q) and trisomy 8 as a subgroup of myelodysplastic syndrome of the type of 5q-syndrome?2014 | First Faculty of Medicine
- Prenatal detection of trisomy 21 on nucleated red blood cells enriched from maternal circulation by using fluorescence in situ hybridization2002 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- QF-PCR Examination of Parental and Meiotic Origin of Trisomy 21 in Central and Eastern Europe2005 | Faculty of Science
- QF-PCR examination of parental and meiotic origin of trisomy 21 in Central and Eastern Europe2005 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Numerical chromosomal changes (monosomy 7, trisomy 8 and trisomy 21) detected by interphase FISH in children with myeloid disordersPublication without faculty affiliation
- Numerical chromosomal aberrations (monosomy 7, trisomy 8 and trisomy 21) ascertained by I-FISH in children with myeloid disordersPublication without faculty affiliation
- Left ventricle shortening fraction: a comparison between euploid and trisomy 21 fetuses in the first trimester2010 | First Faculty of Medicine
- Shortening fraction of the right ventricle: a comparison between euploid and trisomy 21 fetuses at week 11 to week 13 and 6 days of gestation2011 | First Faculty of Medicine
- Differentially expressed miRNAs in trisomy 21 placentas2016 | First Faculty of Medicine
- Choroid plexus cysts and risk of trisomy 18. Modifications regarding maternal age and markers2007 | First Faculty of Medicine
- Mutations in exon 2 of GATA1 are early events in megakaryocytic malignancies associated with trisomy 212003 | Second Faculty of Medicine
- Temporal bone findings in trisomy 18 and 21 syndromes1997 | Publication without faculty affiliation
- A translocation (6;9)(p32;q34) and trisomy 13 in a case of childhood acute nonlymphocytic leukemia1990 | Second Faculty of Medicine
- Histological Investigation of the Temporal Bone in Foetuses with Trisomy of the 21st Chromosome1999 | Publication without faculty affiliation
- Histological Investigation of the Temporal Bone in Foetuses with Trisomy of the 18th Chromosome1999 | Publication without faculty affiliation
- Non-invasive fetal sex determination and screening of trisomy 21 on fetal extracellular DNA and fetal cells enriched from maternal peripheral blood2003 | Central Library of Charles University, Second Faculty of Medicine
- Partial trisomy of 3q detected by chromosome painting in a case of juvenile chronic myelomonocytic leukemia1993 | Second Faculty of Medicine
- A new Down syndrome model: Mice with a partial trisomy of chromosome 17 show cognitive impairmentin the Morris water maze2002 | First Faculty of Medicine
- Slower early response to treatment and distinct expression profile of childhood high hyperdiploid acute lymphoblastic leukaemia with DNA index < 1.162016 | Second Faculty of Medicine
- Down syndrome2011 | Publication without faculty affiliation
- Impact of first trimester screening on Trisomy 21 detection and incidence of invasive procedures in the years 1994-2013 (population based data)Publication without faculty affiliation
- Genome-wide miRNA profiling in plasma of pregnant women with down syndrome fetuses2020 | First Faculty of Medicine
- MoM-based Approach to Noninvasive Prenatal Testing Using Exponentially Weighted Moving Average Chart and Chromosomal Fingerprint2015 | First Faculty of Medicine
- Chromosomal aberrations in the Czech Republic in 1994-2013Publication without faculty affiliation
- Development of acute myeloid leukemia associated with Ph-negative clone with inv(3)(q21q26) during imatinib therapy for chronic myeloid leukemia2009 | Faculty of Medicine in Pilsen