Publikace
- FMR1 Gene Expansion, Large Deletion of Xp, and Skewed X-Inactivation in a Girl With Mental Retardation and Autism2010 | 2. lékařská fakulta
- Molecular cloning and analysis of breakpoints on ring chromosome 17 in a patient with autism2008 | 2. lékařská fakulta
- Identification of a patient with intellectual disability and de novo 3.7 Mb deletion supports the existence of a novel microdeletion syndrome in 2p14-p152013 | 1. lékařská fakulta, Fakulta tělesné výchovy a sportu, 2. lékařská fakulta
- The TP53 gene promoter is not methylated in families suggestive of Li-Fraumeni syndrome with no germline TP53 mutations2009 | 1. lékařská fakulta, Fakulta tělesné výchovy a sportu, 2. lékařská fakulta
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