OGB-RUNX1

Seqplexing

Delivery time

3 weeks

Sample

Blood

270,00€

Familial platelet disorder with associated myeloid malignancy. Somatic mutations are relevant for determining treatment in different tumor types, especially in some leukemias. GENES ANALYZED: RUNX1 (E1-E8). For somatic and germline mutations in blood and paraffin-embedded tissue (5-micron sections) using our proprietary kit.

Other tests

NGS-SEQ+CNVs - POLYPOSIUM SYNDROME-COLORECTAL CANCER

NGS-SEQ+CNVs - POLYPOSIUM SYNDROME-COLORECTAL CANCER

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NGS-SEQ+CNVs - SLE-LIKE SYNDROME

NGS-SEQ+CNVs - SLE-LIKE SYNDROME

520,00€

NGS-SEQ+CNVs - IMMUNODEFICIENCY SYNDROMES

NGS-SEQ+CNVs - IMMUNODEFICIENCY SYNDROMES

650,00€