Nicolaides-Baraitser Syndrome (SMARCA2)
This genetic test detects mutations in the SMARCA2 gene, associated with Nicolaides-Baraitser syndrome. It aids in diagnosing this rare genetic neurodevelopmental disorder characterized by developmental delays and other clinical features.
Also known asNicolaides - Baraitser Syndrome (smarca2) Gene Sequencing Nicolaides - Baraitser Syndrome (smarca2) Gene Sequencing
Test details
Preparations
No special preparations needed
Test included
Nicolaides-Baraitser Syndrome (SMARCA2) includes 1 parameter
- Specimen
Test code
G762
Specimen vol. and vacutainer information
| Specimen | Vacutainer | Volume |
|---|---|---|
| Others (fx) | Others | 2 ML |
Specimen stability information
Others (Fx)
Specimen rejection criteria
Test run frequency
Every Day TIME - 10:00
Turn around time
28 Working Days
Performing locations
Department
- Advanced Molecular Diagnostics R&d
CPT and Loinc codes
Nicolaides-Baraitser Syndrome (SMARCA2)
Package price
₹22000
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₹22000