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: