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
- The Genetics of Autism2002 | Second Faculty of Medicine
- Genetic Study of Twenty Patients with Autism Spectrum Disorders2002 | Second Faculty of Medicine
- Human and Mouse XAP-5 and XAP-5-Like (X5L) Genes: Identification of an Ancient Functional Retroposon Differentially Expressed in Testis1999 | Second Faculty of Medicine
- A complex pattern of evolutionary conservation and alternative polyadenylation within the long 3 '-untranslated region of the methyl-CpG-binding protein 2 gene (MeCP2) suggests a regulatory role in gene expression1999 | Second Faculty of Medicine
- Tumor suppressor genes1997 | Second Faculty of Medicine
- A method for detection of germinal mutations in the p53 tumor suppressor gene1996 | Second Faculty of Medicine
- Disruption of OVOL2 Distal Regulatory Elements as a Possible Mechanism Implicated in Corneal Endothelial Dystrophy2024 | First Faculty of Medicine, Second Faculty of Medicine
- Spliceosome malfunction causes neurodevelopmental disorders with overlapping features2024 | Second Faculty of Medicine
- A new patient with congenital myasthenic syndrome type 20 due to compound heterozygous missense SLC5A7 variants suggests trends in genotype-phenotype correlation2023 | First Faculty of Medicine, Second Faculty of Medicine
- Haploinsufficiency of PRR12 causes a spectrum of neurodevelopmental, eye, and multisystem abnormalities2021 | First Faculty of Medicine, Second Faculty of Medicine
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