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Hemostaseology

We perform molecular genetic investigation of the hereditary coagulation disorders listed below.
Please use our Request form when sending samples.

If you require further information please do not hesitate to contact us.

Disease (gene) Method Material Processing time
Antithrombin III deficiency (SERPINC1) Sequencing (complete) & MLPA EDTA blood 2-3 weeks
Protein C deficiency (PROC) Sequencing (complete) & MLPA EDTA blood 2-3 weeks
Protein S deficiency (PROS1) Sequencing (complete) & MLPA EDTA blood 2-3 weeks
Afibrinogenemia (FGA)* Sequencing (complete) EDTA blood / DNA 2-3 weeks
Afibrinogenemia (FGB)* Sequencing (complete) EDTA blood / DNA 2-3 weeks
Afibrinogenemia (FGG)* Sequencing (complete) EDTA blood / DNA 2-3 weeks
Factor II deficiency (F2) Sequencing (complete) EDTA blood / DNA 2-3 weeks
Factor V deficiency (F5)* Sequencing (complete) EDTA blood / DNA 3-4 weeks
Factor VII deficiency (F7) Sequencing (complete) EDTA blood / DNA 2-3 weeks
Hemophilia A (F8)* 1. PCR analysis (IVS22-A inversion & IVS1 inversion)
2. Sequencing (complete) & MLPA
EDTA blood 1. 2-3 weeks
2. 2-3 weeks
Hemophilia B (F9) Sequencing (complete) & MLPA EDTA blood 2-3 weeks
Factor X deficiency (F10)* Sequencing (complete) EDTA blood / DNA 2-3 weeks
Factor XI deficiency (F11)* Sequencing (complete) EDTA blood / DNA 2-3 weeks
Factor XII deficiency (F12)* Sequencing (complete) EDTA blood / DNA 2-3 weeks
Factor XIII, A subunit deficiency (F13A1)* Sequencing (complete) EDTA blood / DNA 2-3 weeks
Factor XIII, B subunit deficiency (F13B)* Sequencing (complete) EDTA blood / DNA 2-3 weeks

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