FISH (Fluorescence In Situ Hybridization)
The Cytogenetics Laboratory at UCSD is currently offering FISH analysis for the following disorders. Each test in the menu includes information on indications for testing, assay methodology, specimen requirements, transport and shipping instructions, and billing codes. All specimens submitted for analysis should be accompanied by the UCSD Medical Genetics Laboratories Test Requisition Form.
Constitutional Studies
- 1p36 Microdeletion syndrome
- Angelman syndrome
- Cri du Chat syndrome
- DiGeorge/VCFS syndrome
- Fetal Aneuploidy Screen
- Miller-Dieker syndrome
- Prader-Willi syndrome
- Smith-Magenis syndrome
- STS/Kallman syndrome
- Williams syndrome
- Wolf-Hirschhorn syndrome
Oncology Studies
- CLL Analysis
- ALL Analysis
- AML Analysis
- MDS Analysis
- Multiple Myeloma Analysis
- Lymphoma Analysis
- BCL6 Flanking probes - 3q27
- ALK – 2p23
- EGR1 – 5q31
- PDGFRB – 5q32
- D7S486 – 7q31
- RUNX1T1/RUNX1 – t(8;21)
- BCR/ABL Fusion – t(9;22)
- TRA/D – 14q11.2
- RARA –t(15;17)
- CBFB – inversion 16
- CCND/IGH Fusion – t(11;14)
- DDIT3 Flanking probes – 12q13
- FIP1L1/CHIC2/PDGFRA Fusion – 4q12
- IGH/BCL2 Fusion – t(14;18)
- IGH/FGFR3 Fusion – t(4;11)
- IGH/MAF Fusion – t(4;16)
- IGH/MALT1 Fusion – t(14;18)
- MLL Flanking probes (11q23)
- MYC Flanking probes (8q24)
- ETV6/RUNX1 Fusion – t(12;21)
- E2A – 19p13.3
- EWSR1 – 22q12
- XX/XY Sex Mismatch