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Test Code:
090-71-3006-01

Order Name:
DNA for Fragile X Syndrome **

 
Useful For:

Confirmation of a diagnosis of fragile X syndrome (FMR1 gene mutation)

 
Methodology:
Fluorescent based PCR technique using capillary electrophoresis and fluorescent based MS-PCR technique
 
AliasesName:
FMR1 gene mutation
 
 
 
Test Code:
090-71-3006-01

Order Name:
DNA for Fragile X Syndrome **

 
Patient Preparation:
N/A
 
Collection Specimen Or Container:
Blood/ EDTA Blood (Lavendor Top) 3 mL, 2 tubes

Document Required
Filled Requisition Form of Ramathibodi Human Genetic laboratory
 
Specimen Testing Type:
Whole blood EDTA, minimum volume 3-5 mL
 
Sub Mission Container:
Original tube
 
 
 
Test Code:
090-71-3006-01

Order Name:
DNA for Fragile X Syndrome **

 
Method detail:
Fluorescent based PCR technique using capillary electrophoresis and fluorescent based MS-PCR technique
 
Schedule:
N/A **Sent Out to Ramathibodi
 
Turnaround Time:
Received specimen to reported within 30 days
(Exception for official holidays)
 
Performing Location:
Ramathibodi
Referral Lab Services, Laboratory Department 14160-2
 
 
 
Test Code:
090-71-3006-01

Order Name:
DNA for Fragile X Syndrome **

 
 
Reference Value: