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We published three case reports in Acta medicinae
In the latest issue of the journal Acta medicinae, a team of doctors and colleagues from the GHC Genetics laboratory published the following case reports:
- Double homozygote of severe thrombophilic mutations
- Genetic heterogeneity and phenotypic variability of hereditary cancer syndromes
- Neurofibromatosis type 1 - a genetically determined multisystem disease detected in a patient in the context of a diagnosis of breast cancer
The full text of the case reports can be found in the appendix: