Publikace
- CNVs in patients with epilepsy - Czech experiencePublikace bez příslušnosti k fakultě
- The Human Phenotype Ontology in 2024: phenotypes around the world2024 | 2. lékařská fakulta
- Genetic testing in children enrolled in epilepsy surgery program. A real-life study2023 | 2. lékařská fakulta, Ústřední knihovna
- Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood2022 | 2. lékařská fakulta
- Genetic Testing for Malformations of Cortical Development2022 | 2. lékařská fakulta
- Monozygotní dvojčata s Legius syndromem a diferenciální diagnostika Legius syndromu a neurofibromatózy typ 12021 | 2. lékařská fakulta
- Male patient with ALG13 associated congenital disorder of glycosylation2021 | 2. lékařská fakulta
- Importance of the integrated test in the Down's syndrome screening algorithm2018 | 2. lékařská fakulta, 1. lékařská fakulta
- A boy with developmental delay and mosaic supernumerary inv dup(5)(p15.33p15.1) leading to distal 5p tetrasomy - case report and review of the literature2018 | 2. lékařská fakulta
- Molecular Cytogenetic Diagnostics of Marker Chromosomes: Analysis in Four Prenatal Cases and Long-Term Clinical Evaluation of Carriers2018 | 2. lékařská fakulta
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