Osmolality, Serum
Very Long Chain Acyl-CoA Dehydrogenase Deficiency, Gene Mutation Analysis
Helicobacter pylori Antibody, IgA, IgG, IgM
Respiratory Viral Pathogen Panel, Molecular
Rheumatoid Factor (RF)
Antipsychotics (Neuroleptics) Class
Amoxapine, Urine
Microsomal epoxide hydrolase 1 (EPHX1) Gene Variation
Homovanillic Acid (HVA), Random, Urine
Pregnenolone
LDS
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TNF receptor superfamily member 13B 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
TNF receptor superfamily member 13B Gene Mutation Analysis
Medical Test
Additional Testing
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TNF receptor superfamily member 13B Gene Mutation Analysis
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