Description
The FISH (Fluorescence In Situ Hybridization) test for Chronic Lymphocytic Leukemia (CLL) is designed to identify specific chromosomal abnormalities that have prognostic significance. The “1 set” likely refers to a panel of probes targeting specific chromosomal regions: deletion of 13q (13q14), trisomy 12, and deletions of TP53 (17p13) and ATM (11q22-23). These abnormalities are frequently found in CLL and are associated with different prognoses.



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