Gerinnung / Hämatologie

Hereditäre Sphärozytose, ID 603.00 (5 Gene)

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Hermansky Pudlak Syndrom und Differentialdiagnosen (Chediak-Higashi-, Griscelli-Syndrom), ID 720.01 (15 Gene)

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Hyperhomocysteinämie (MTHFR, C677T) (1 Gene)

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Makrothrombozytopenie - Basisdiagnostik, ID 721.00 (10 Gene)

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MTHFR c.665C>T und c.1286A>C (1 Gene)

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Sichelzellanämie (HBB, p.Glu7Val) (1 Gene)

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Thalassämie-beta, HBB (1 Gene)

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Thalassemia, alpha, HBA1, HBA2 (1 Gene)

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Thrombophilie, Faktor-II (Prothrombin, F2) c.20210G>A (1 Gene)

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Thrombophilie, Faktor-V-Leiden (F5) c.1601G>A (1 Gene)

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Thrombozytopathie - Basisdiagnostik, ID 719.00 (11 Gene)

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Thrombozytopathie und Thrombozytopenie - Gesamtpanel, ID 722.01 (90 Gene)

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Thrombozytopenie, ID 607.00 (10 Gene)

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Thrombozytopenie - Basisdiagnostik, ID 718.00 (8 Gene)

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