SRD 1p36, (FISH)
On demand
Order number :
ST-F06
Detection of 1p36 deletion
Main indication:
Neuroblastoma.
Test usage:
1p36 FISH (fluorescence in situ hybridization) is offered for diagnosis of individuals with clinical features of 1p36 deletion syndrome, including craniofacial abnormalities, developmental delay, hypotonia, learning disability, hearing loss, heart problems, and seizures. The detection rate of FISH analysis for this disorder is approximately 95%.
NO related applications
There are no report
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