ACHONDROPLASIA (FGFR3 FULL GENE SEQUENCING)

This genetic test sequences the FGFR3 gene to diagnose achondroplasia, a form of dwarfism caused by mutations in this gene.

Also known asFgfr3 Achondroplasia (fgfr3 Full Gene Sequencing) Achondroplasia (fgfr3 Full Gene Sequencing)

Available via

Home Collection, Lab Visit

Contains

1 parameters

Earliest reports in

21 Working Days

Test details
Preparations

No special preparations needed

Test included
ACHONDROPLASIA (FGFR3 FULL GENE SEQUENCING) includes 1 parameter

  • Achondroplasia (fgfr3 Full Gene Sequencing)

Test code

G512

Specimen vol. and vacutainer information
SpecimenVacutainerVolume
Amniotic FluidPlain Sterile Vaccutainer 3 ML
Peripheral BloodOthers3 ML

Specimen stability information

Amniotic Fluid, Peripheral Blood

Specimen rejection criteria

Test run frequency

Every Day TIME - 10:00

Turn around time

21 Working Days

Performing locations

Department

  • Advanced Molecular Diagnostics R&d

CPT and Loinc codes

ACHONDROPLASIA (FGFR3 FULL GENE SEQUENCING)

20000