Instructions: 7-10mL whole blood in green sodium heparin, ambient. Min 2.0mL. Alt 2mL
bone marrow in sodium heparin, ambient. Min 1.0mL.
Text: Useful for Detecting a neoplastic clone associated with the common
chromosome anomalies seen in patients with acute leukemia or other
myeloid malignancies; Tracking known chromosome abnormalities in
patients with myeloid malignancies thus assessing their response to
therapy. Useful when standard cytogenetic analysis is unsuccessful.
Methodology: Fluorescence In Situ Hybridization (FISH)
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