Test ID: FRTEL
Subtelomeric Region Anomalies, FISH
Method Description
Describes how the test is performed and provides a method-specific reference
The subtelomere-specific FISH test is done with commercially available DNA fluorescent probes for each chromosome. Each chromosome is separately analyzed. At least 3 metaphases are analyzed with each p-arm and q-arm probe pair. A total of 41 telomere-specific probes are used. These probes hybridize specifically to the respective TAR region of each chromosome, with the exception of the 5 p-arms of acrocentric chromosomes, which do not have unique sequences. The processing time is usually 24 hours, and the test can be performed on cultured lymphocytes or fibroblasts. (Jalal SM, Harwood AR, Sekhon GS, et al: Utility of subtelomeric fluorescent DNA probes for detection of chromosome anomalies in 425 patients. Genet Med 2003;5:28-34)
Day(s) and Time(s) Test Performed
Outlines the days and times the test is performed. This field reflects the day and time the sample must be in the testing laboratory to begin the testing process and includes any specimen preparation and processing time required before the test is performed. Some tests are listed as continuously performed, which means assays are performed several times during the day.
Samples processed Monday through Sunday. Results reported Monday through Friday, 8 a.m.-5 p.m. CST.


