Myoglobin, Serum
India Ink Preparation, CSF
Adrenocorticotropic Hormone (ACTH)
Biopsy, Lymph Node
Listeria Antibody, Serum
Galactose-1-Phosphate Uridyltransferase, Blood
Bone Alkaline Phosphatase, Serum
Hemoglobin, Qualitative, Urine
Cryptococcus Antigen, Serum
Epstein-Barr Virus (EBV) VCA, IgM

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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

Turnaround Time

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