Phospholipid (Cardiolipin) Atnibody, IgA
Norfentanyl, Urine
HIV1/HIV2 Antibody Differentiation
Tobramycin, Serum
Isocitrate Dehydrogenase 1 (IDH1) Mutation Analysis
Phenobarbital, Confirmation, Urine
Gram Stain, Sputum
Neuromyelitis optica spectrum disorders (Devic disease)
Hereditary Peripheral Neuropathies Gene Mutation Panel, NGS
Special Stain, Congo Red

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LDS
/Medical Tests
/Hypochondroplasia (FGFR3) Gene Mutation Analysis

All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References

All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References

Hypochondroplasia (FGFR3) Gene Mutation Analysis
Medical Test

Specimen Collection

Access to Hypochondroplasia (FGFR3) Gene Mutation Analysis is restricted.