Oncogenetic testing, diagnosis and follow-up in Birt-Hogg-Dubé syndrome, familial atypical multiple mole melanoma syndrome and neurofibromatosis 1 and 2
- MeSH Terms
- Genetic Testing (E01.370.225.562); Genetic Predisposition to Disease (C23.550.291.687.500)
- Publication Scope
- counselling
- management
- Countries of Application
- Belgium
- Guideline Publication Status
- Published
- Languages
- English
- Authors
- KCE (BE)
- Publication Year
- 2015