THALASSEMIA BETA TRIO PRENATAL MUTATION DETECTION
This test is useful for detection of mutations in the HBB gene linked to Beta Thalassemia. This assay detects more than 100 different mutations in the Promoter region, Exon 1, IVS-I & Exon 2 and part of IVS-II OF THE HBB Gene. It also detects the deletion of 690 bp in IVS II and Exon 3. . This assay checks for maternal cell contamination in amniotic fluid.
Parameter(s) covered : 3
Report Frequency: Sample Mon by 11 am; Report Fri
Special Instruction: Duly filled Form G, Prenatal Genetic testing Consent Form (Form 18) and Physician prescription is mandatory. Samples shall be accepted only from registered genetics clinics under PCPNDT Act.
Price : ₹ 18000.00
Parameters
- Amniotic Fluid
- Husband
- Wife