Publications
- Application of DNA microarray - gene expression studies in pathological statesPublication without faculty affiliation
- Analysis of nucleic acids using DNA microarray technologyPublication without faculty affiliation
- Making DNA microarrays - optimisation and comparison of various DNA immobilisation strategiesPublication without faculty affiliation
- 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 | First Faculty of Medicine
- 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 deficiencyPublication without faculty affiliation
- A Primary Transcript Map for the Familial Juvenile Hyperuricemic Nephropathy (FJHN) Critical Region on Chromosome 16p11. 2Publication without faculty affiliation
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