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Short tandem repeat
Publication
Class
Person
Publication
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publication
Allele frequency data for 17 short tandem repeats in a Czech population sample
2009 |
Faculty of Education
publication
Allele frequency data for 17 short tandem repeats in a Czech population sample
2009 |
Faculty of Science, Faculty of Education, First Faculty of Medicine
publication
Allele frequency data for 17 short tandem repeats in a Czech population sample
2009 |
First Faculty of Medicine
publication
Evaluation of 14 Y-chromosomal short tandem repeat haplotype with focus on DYS449, DYS456, and DYS458: Czech population sample
2010 |
Faculty of Science, Faculty of Education
publication
Evaluation of 14 Y-chromosomal short tandem repeat haplotype with focus on DYS449, DYS456, and DYS458: Czech population sample
2010 |
Faculty of Science, Faculty of Education, First Faculty of Medicine, Faculty of Mathematics and Physics
publication
Toward Male Individualization with Rapidly Mutating Y-Chromosomal Short Tandem Repeats
2014 |
Second Faculty of Medicine
publication
Allele frequency data for 17 short tandem repeats in a Czech population sample
2009 |
Publication without faculty affiliation
publication
OmniPlex-a new QF-PCR assay for prenatal diagnosis of common aneuploidies based on evaluation of the heterozygosity of short tandem repeat loci in the Czech population
2008 |
Second Faculty of Medicine
publication
People "on the Margin": A Medieval Cemetery in Český Brod - Malechov (Central Bohemia)
2017 |
Faculty of Science, Second Faculty of Medicine
publication
Genetic Structure of Pastoral and Farmer Populations in the African Sahel
2011 |
Faculty of Science
publication
DNA Analysis of Ancient Skeletal Remains
2010 |
Faculty of Science
publication
HVRII of mtDNA in Cord Blood Cells of Newborn Children and in Their Saliva 10 Years Later
2011 |
Faculty of Science
publication
Preimplantation genetic diagnostics of monogenic-based diseases: possibilities, pitfalls and first accomplishments in the Czech Republic
2008 |
Second Faculty of Medicine
publication
Molecular genetic investigation of polymorfisms and STR loci in patients with nonsmall cell lung cancer
2009 |
First Faculty of Medicine
publication
The novel contiguous gene syndrome of myotubular myopathy (MTM1), male hypogenitalism and deletion in Xq28: report of the first familial case
1999 |
Second Faculty of Medicine
publication
Detection of deletions and uniparental disomies in Prader-Willi and Angelman syndromes - methodical and interpretational aspects
2000 |
Second Faculty of Medicine
publication
Investigative genetic genealogy - new approach to detect relatedness of individuals
2021 |
First Faculty of Medicine
publication
Should Patients with Kearns-Sayre Syndrome and Corneal Endothelial Failure Be Genotyped for a TCF4 Trinucleotide Repeat, Commonly Associated with Fuchs Endothelial Corneal Dystrophy?
2021 |
First Faculty of Medicine
publication
Case report: type 1 diabetes in monozygotic quadruplets
2012 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
publication
Complex analysis of 700-Year-Old Skeletal Remains found in an Unusual Grave-Case Report
2015 |
Faculty of Science
publication
Analysis of 8 X-chromosomal markers in the population of central Croatia
2013 |
First Faculty of Medicine
publication
Y-chromosomal diversity of the Valachs from the Czech Republic: model for isolated population in Central Europe
2011 |
Second Faculty of Medicine
publication
Spectrum of CFTR mutations in Chechen cystic fibrosis patients: high frequency of c.1545_1546delTA (p.Tyr515X; 1677delTA) and c.274G > A (p.Glu92Lys, E92K) mutations in North Caucasus
2019 |
Second Faculty of Medicine