Test description
Fluorescence in-situ hybridisation (FISH) can be used in conjunction with conventional or microarray analysis for the investigation of specific chromosomal syndromes. Available tests are listed below.
The suspected clinical condition for which testing is being sought must be included on the request form.
Test information
Test name
Targeted FISH for neonatal diagnosis of aneuploidy
Clinical indication
For neonatal diagnosis of suspected chromosomal syndromes
Gene(s)
Chromosomes X , Y, 13, 18 and 21
Method
FISH
Turn around time
2 days
Medicare eligibility
Price
If not MBS eligible, please contact 1800 822 999 for pricing details
Test request form
Standard pathology request form
Sample type
Blood
Collection type
Min 1mL in 1 x paediatric Lithium heparin tube
Special instructions
Test is performed with conventional chromosome analysis. No additional sample required.