NABL Accredited
Trisomy (Aneuploidy) for Chromosome (13 & 21), Cord blood
Sample Collection & Prep:
3 ml of Prenatal Cord Blood In Na-Heparin Vacutainer .This code is only for prenatal cord blood and not for POC cord blood
Specimen Type:
Whole Blood (EDTA/Heparin)
Testing Methodology:
Fluorescence In Situ Hybridization (FISH) 3 ml
Testing Schedule:
Mon–Sat 6th Day 06:00 PM
Report Delivery:
Within 6th day via WhatsApp & Email
Fasting Requirement:
No strict fasting required before sample collection
Quality Standard:
100% NABL Accredited clinical reference laboratory testing
Clinical Instructions:
Detailed clinical history including anomaly scan report must be submitted with sample, Doctor's Prescription with doctor name and contact number, Maternel screening reports if available, Consent Form (Form G) as per PCPNDT mandatory, Sample forwarding letter also mandatory
₹5340
Test Information
Preparation requirements and diagnostic clinical parameters.
Parameters
1 Parameter- 1 diagnostic parameter
- Automated calibrated clinical analyzer
Fasting & Prep
No Fasting- No strict fasting required
- Plain drinking water intake permitted
Specimen
Whole Blood (EDTA/Heparin)- Matrix: Whole Blood (EDTA/Heparin)
- Prep: 3 ml of Prenatal Cord Blood In Na-Heparin Vacutainer .This code is only for prenatal cord blood and not for POC cord blood
Turnaround
6th day- Report in Mon–Sat 6th Day 06:00 PM
- Verified PDF via WhatsApp & Email
Trisomy (Aneuploidy) for Chromosome (13 & 21), Cord blood
1 parameter across 1 body system
Blood & Hematology Health
Analyzes blood cells, hemoglobin levels, and cellular health markers.
1 Parameter
Trisomy (Aneuploidy) for Chromosome (13 & 21), Cord blood
Trisomy (Aneuploidy) for Chromosome (13 & 21), Cord blood
