THIS TEST IS USED FOR THE DETECTION OF ABNORMALITIES DUE TO INV 16 (P13Q22) / T (16;16)(P13;Q22) [CBFB-MYH11] WHICH ARE ASSOCIATED WITH ACUTE MYELOID LEUKEMIA.
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3 ML (2 ML MIN.) WHOLE BLOOD / BONE MARROW FROM 1 LAVENDER TOP (EDTA) TUBE. SHIP REFRIGERATED. DO NOT FREEZE. DULY FILLED GENOMICS CLINICAL INFORMATION REQUISITION FORM IS MANDATORY.
REAL TIME PCR
REPORT ON 15TH DAY EVENING 7PM
DULY FILLED GENOMICS CLINICAL INFORMATION REQUISITION FORM IS MANDATORY.