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Clear
 
Test Code:
090-71-8502

Order Name:
Prader-Willi/Angelman syndrome by MS-MLPA **

 
Useful For:
ช่วยระบุกลไกของการเกิดโรคของกลุ่มอาการ Prader-Willi/Angelman ได้ทั้ง methylation, deletion และ duplication
 
Methodology:
Methylation-Specific Multiplex Ligation-dependent Probe Amplification (MS-MLPA)
 
AliasesName:
Nucleophosmin Mutation Analysis
 
 
 
 
Test Code:
090-71-8502

Order Name:
Prader-Willi/Angelman syndrome by MS-MLPA **

 
Collection Specimen Or Container:
Blood/ K3 EDTA (Lavender Top) 3 mL, 2 tubes
 
 
Specimen Testing Type:
EDTA Whole blood, minimum volume 3 mL
 
Sub Mission Container:
Original tube
 
 
 
Test Code:
090-71-8502

Order Name:
Prader-Willi/Angelman syndrome by MS-MLPA **

 
Method detail:
Methylation-Specific Multiplex Ligation-dependent Probe Amplification (MS-MLPA)
 
Schedule:
N/A **Send out to Human Genetics, Ramathibodi
 
 
Turnaround Time:
Received specimen to reported within 17 days
(Exception for official holidays)
 
 
Performing Location:
Human Genetics, Ramathibodi
Referral Lab Services, Laboratory Department 14160-2
 
 
 
Test Code:
090-71-8502

Order Name:
Prader-Willi/Angelman syndrome by MS-MLPA **

 
 
Clinical Reference:
Ramathibodi Laboratory Guide book