Publikace
- Application of DNA microarray - gene expression studies in pathological statesPublikace bez příslušnosti k fakultě
- Analysis of nucleic acids using DNA microarray technologyPublikace bez příslušnosti k fakultě
- Making DNA microarrays - optimisation and comparison of various DNA immobilisation strategiesPublikace bez příslušnosti k fakultě
- Familial juvenile hyperuricaemic nephropathy (FJHN): linkage analysis in 15 families, physical and transcriptional characterisation of the FJHN critical region on chromosome 16p11.2 and the analysis of seven candidate genes2003 | 1. lékařská fakulta
- Novel mutation in genes for frequent X-linked metabolic diseases (X-ALD, Fabry disease, OTC deficiency). A prevalent mutation for late onset form of OTC deficiencyPublikace bez příslušnosti k fakultě
- A Primary Transcript Map for the Familial Juvenile Hyperuricemic Nephropathy (FJHN) Critical Region on Chromosome 16p11. 2Publikace bez příslušnosti k fakultě
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