Background
FISH, a molecular cytogenetic technique, enables the analysis of disease specific abnormalities. It is offered for the detection of cryptic rearrangements, microdeletion syndromes, aneuploidy, and marker chromosome identification.
This branch of cytogenetic analysis is more specific than standard karyotype analysis, enabling analysis of disease-specific abnormalities. Using results from previous testing, specific gene locations can be selected for investigation. FISH is offered for the detection of translocations, microdeletion syndromes, aneuploidy and marker chromosome identification.
Fluorescence in-situ Hybridization Tests
A-Z FISH test menu
ALK 2p23 rearrangement by FISH
AML1(RUNX1)/ETO(RUNXT1) t(8;21) by FISH
Angelman Syndrome deletion 15q11-13 by FISH*
API2/MALT1 t(11;18) by FISH*
ATM/CEP11 deletion 11q22.3 by FISH
BCL6 3q27 Rearrangement by FISH
BCR/ABL1 t(9;22) by FISH
Bladder Cancer Panel +3,+7,+17,9p21- by FISH
Burkitt/“Double Hit” Large B-cell Lymphoma Panel by FISH
C MYC 8q24 Rearrangement by FISH
CBFB t(16;16), inv(16) by FISH
Chronic Lymphocytic Leukemia (CLL) Panel by FISH
Cri-du-Chat / SOTOS Syndrome by FISH*
Deletion 13q14.3 by FISH
Deletion 20q12 by FISH
deletion 7q22 by FISH
DiGeorge/Velo-Cardio-Facial Syndrome deletion 22q11.2 by FISH*
EGFR amplification (7p11.2) by FISH*
EGR1 5q deletion, monosomy 5 by FISH
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