- Analysis of paternal alleles in nucleated red blood cells enriched from maternal blood2001 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Substitution in the promoter region ofthe CYP21 affects a phenotype ofthe disease in patients with 21-hydroxylase deficiency2009 | Third Faculty of Medicine
- Changes on chromosome 11p15.5 as specific marker for embryonal rhabdomyosarcoma?2023 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine, Third Faculty of Medicine, Central Library of Charles University
- Prader-Willi syndrome due to uniparental disomy in a patient with a balanced chromosomal translocation2006 | Second Faculty of Medicine
- Spinal muscular atrophy caused by a novel Alu-mediated deletion of exons 2a-5 in SMN1 undetectable with routine genetic testing2020 | First Faculty of Medicine