Publications
- EuroGentest: an EU-funded Project for Harmonisation and Improvement of the Quality of Genetic Services2007 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- Prader-Willi syndrome due to uniparental disomy in a patient with a balanced chromosomal translocation2006 | Second Faculty of Medicine
- Diagnostic possibilities of Prader-Willi and of Angelman syndromes2005 | Second Faculty of Medicine
- Concomitancy of mutation in FRDA gene and FMR1 premutation in 58 year-old woman2005 | Second Faculty of Medicine
- Quantitative fluorescent PCR (QFPCR) in the examination of microquantity of fetal cells2002 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- Genetic Study of Twenty Patients with Autism Spectrum Disorders2002 | Second Faculty of Medicine
- Detection of deletions and uniparental disomies in Prader-Willi and Angelman syndromes - methodical and interpretational aspects2000 | Second Faculty of Medicine
- DNA diagnosis of the fragile X chromosome syndrome - FRAXA using PCR1998 | Second Faculty of Medicine
- DNA diagnostika onemocnění způsobených amplifikací triplet repetitivních sekvencí1995 | Second Faculty of Medicine, Central Library of Charles University
- DNA diagnostika vrozených poruch metabolismu +11995 | Second Faculty of Medicine, Central Library of Charles University
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