Classes
- Medical Biology I +1D0102337 | Second Faculty of Medicine
- Lékařská biologie II +1D0103039 | Second Faculty of Medicine
- Medical biology and human geneticsD09010005 | Second Faculty of Medicine
- Cell +1D1101001 | Second Faculty of Medicine
- Biology I. +1D1102338 | Second Faculty of Medicine
- Biology II. +1D1103040 | Second Faculty of Medicine
- Medical biology I +1DA0102337 | Second Faculty of Medicine
- Medical Biology II +1DA0103039 | Second Faculty of Medicine
- OS - Advances in Molecular Genetics +1DV01079 | Second Faculty of Medicine
Publications
- 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 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- A patient with de novo 0.45Mb deletion of 2p16.1: The role of BCL11A, PAPOLG, REL, and FLJ16341 in the 2p15-p16.1 microdeletion syndrome2013 | Second Faculty of Medicine
- Chromosome 12q13.13 deletions involving the HOXC gene cluster: Phenotype and candidate genes2013 | Second Faculty of Medicine
- Li-Fraumeni Syndrome2003 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Significance of TP53 gene identification in tumour affected families2003 | Second Faculty of Medicine
- A Li-Fraumeni syndrome family with retained heterozygosity for a germline TP53 mutation in two tumours2003 | Second Faculty of Medicine
- Genetic Study of Twenty Patients with Autism Spectrum Disorders2002 | Second Faculty of Medicine
- Is there anticipation in the age at onset of cancer in families with Li-Fraumeni syndrome?2002 | Second Faculty of Medicine
- Heretidary predisposition to cance: the Li-Fraumeni syndrome as an example2000 | Second Faculty of Medicine
- A database of germline p53 mutations in cancer-prone families1998 | Second Faculty of Medicine
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