BOHRING-OPITZ SYNDROME (ASXL1) GENE SEQUENCING
A genetic test used to identify mutations in the ASXL1 gene, responsible for Bohring-Opitz syndrome, a rare disorder characterized by developmental delay and distinct facial features.
Also known asBohring-opitz Syndrome (asxl1) Gene Sequencing Bohring-opitz Syndrome (asxl1) Gene Sequencing
Test details
Preparations
No special preparations needed
Test included
BOHRING-OPITZ SYNDROME (ASXL1) GENE SEQUENCING includes 1 parameter
- Specimen
Test code
G684
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
BOHRING-OPITZ SYNDROME (ASXL1) GENE SEQUENCING
Package price
₹22000
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₹22000