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FISH for Other Malignancies

 

Our laboratory can also provide FISH analysis for chromosome changes that have been found in other malignancies.

n-MYC 2p24 amplification in neuroblastoma
TCR alpha/delta 14q11
PDGFRB/TEL t(5;12)
MYB 6q23
ETV6  12p13 rearrangement
c-MYC 8q24 rearrangement
TP53 17p13 deletion
BCL2 18q21 rearrangement
FIP1L1 4q12 rearrangement
D13S25 13q14.3
CCND1 11q13 rearrangement
CSF1R 5q33-q34
ALK 2p23 rearrangement
EWSR1 22q12 Ewing sarcoma
FKHR 13q14 rhadomyosarcoma
FUS 16p1.2 myxoid/round cell liposarcoma
CHOP 12q13 myxoid/round cell liposarcoma
SS1 18q11.2 synovial sarcoma
MDM2 12q15 differentiated liposarcoma
ERBB2 (HER2/neu)amplification in breast cancer
ROS1 6q22 rearrangement
EGFR 7p12 amplification
1p/del(19q) oligodendrogliomas
RB1 13q14 deletion
Wilms tumor

Methodology: Fluorescent in Situ Hybridization (FISH) Analysis

Purpose: Confirmation of Clinical Diagnosis/Monitor During Treatment

Test Requisition: Cancer Requisition

Turn-around-time: 2-5 days

Specimen Requirements

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Contact Information
Genetics Laboratory
University of Oklahoma Health Sciences Center
1122 NE 13 Street, Suite 1400, Oklahoma City, OK 73104
Phone: (405) 271-3589 |Fax: (405) 271-7117 Email: Dr. Shibo Li

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