For Hematology/Oncology see Oncology section Hematology
CGC Mutation Panels
- Thrombophilia and Warfarin Pharmacogenetics
Molecular Cytogenetics
- FISH analysis of sexual chromosomes (X/Y)
- FISH analysis with centromeric probe
- FISH analysis with painting probe
- FISH analysis with subtelomeric probe
- FISH analysis with unique sequence probe
Molecular Diagnostics
- Chimerism after bone marrow transplantation
- Drug metabolism (CYP2D6, CYP2C9, CYP2C19, CYP3A4 and NAT2 genes)
- Hereditary Hemochromatosis (frequent mutations of HFE gene)
- Thrombophilia marker Antithrombin III (sequence analysis of SERPINC1 gene)
- Thrombophilia marker APOE (allels 2, 3 and 4)
- Thrombophilia marker Factor II (G20210A)
- Thrombophilia marker Factor V Leiden (R506Q)
- Thrombophilia marker FGB (-455G/A)
- Thrombophilia marker MTHFR (C677T and A1298C)
- Thrombophilia marker PAI-1 (4G/5G)
- Thrombophilia marker Protein C deficiency (sequence analysis of PROC gene)
- Thrombophilia marker Protein S deficiency (sequence analysis of PROS1 gene)
- Thrombophilia and Warfarin Pharmacogenetics See CGC Mutation Panel
