BORJESON-FORSSMAN-LEHMANN SYNDROME (PHF6)
This genetic test identifies mutations in the PHF6 gene, responsible for Borjeson-Forssman-Lehmann syndrome, a rare X-linked intellectual disability disorder.
Also known asBorjeson-forssman-lehmann Syndrome (phf6) Gene Sequencing Borjeson-forssman-lehmann Syndrome (phf6) Gene Sequencing
Test details
Preparations
No special preparations needed
Test included
BORJESON-FORSSMAN-LEHMANN SYNDROME (PHF6) includes 1 parameter
- Specimen
Test code
G722
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
BORJESON-FORSSMAN-LEHMANN SYNDROME (PHF6)
Package price
₹22000
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₹22000