세포유전(T.5952)
- C6001000: Chromosome analysis, constitutional anomaly
- C6005000: Chromosome analysis, hematologic malignancy
- CX568006: Chromosome analysis, Lymph node
- BFL00002: Chromosome analysis, amniotic fluid
- BFL00003: Chromosome analysis, chorionic villi
- GBF00001: AML panel FISH
- CZ967023: FISH, X & Y
- GBF00002: ALL panel FISH
- CZ967026: FISH_bcr/abl
- GBF00003: MDS panel FISH
- GBF00004: Eosinophilia panel FISH
- CZ967027: FISH, PML/RARA
- CZ967033: FISH, RARA BAP
- CZ967031: FISH, AML1/ETO
- CZ967014: FISH, TEL/AML1
- CZ967013: FISH, trisomy13 (Patau syndrome)
- CZ967001: FISH, trisomy18 (Edwards syndrome)
- CZ967002: FISH, trisomy21 (down syndrome)
- CZ967022: FISH, Williams-Beuren syndrome
- CZ967006: FISH, Prader-Willi/Angelman syndrome
- CZ967007: FISH, CATCH22 syndrome
- CZ967032: FISH, CBFB/MYH11
- CZ967030: FISH, MLL BAP
- CZ967028: FISH, P16/CEP9
- CZ967029: FISH, MYC BAP
- CZ967035: FISH, D13S319/LAMP1
- CZ967036: FISH, P53/CEP17
- GBF00005: MM panel FISH
- CZ967034: FISH, IGH-BAP
- CZ967003: FISH, IGH/FGFR3
- CZ967004: FISH, IGH/CCND1 XT
- CZ967005: FISH, IGH/MAF
- CZ967009: FISH, IGH/BCL2
- CZ967012: FISH, IGH/MYC, CEP8
- CZ967008: FISH, IGH/MALT1
- CZ967010: FISH, ALK-BAP
- CZ967011: FISH, BCL6-BAP
- CZ967017: FISH, EGR-1/D5S721;D5S23
- CZ967016: FISH, D7S486/CEP7
- CZ967015: FISH, D20S108/TelVysion 20P
- CZ967018: FISH, FIP1L1-PDGFRA
- CZ967020: FISH, PDGFRB-BAP
- CZ967021: FISH, FGFR1-BAP
- CZ967019: FISH, 1p36/1q21
- CZ967042: FISH, ATM/CEP11
- GBF00008: FISH, CLL panel