1p36.3 Microdeletion Syndrome, FISH
Aminolevulinic Acid, Urine
Fabry Disease (GLA) Gene Mutation Analysis
Cortisol/Cortisone, Free, 24 Hour, Urine
Lysozyme (Muramidase), Serum
Tricyclic Antidepressant (TCA), Urine
Hepatitis B Core Antibody, IgM
ASXL3 Gene Mutation Analysis
Allergen Specific IgE, Mold (Allergens) Panel
von Willebrand Disease 2N (Subtype Normandy), Genotyping
LDS
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Culture, Vibrio, Stool
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All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References
Culture, Vibrio, Stool
Medical Test
Methodology
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