Prolyl Hydroxylase Domain-2 (PHD2/EGLN1) Gene Mutation Analysis
Chromosome Analysis, Body Fluid
Williams Syndrome, 7q11.23 Deletion
Vascular Endothelial Growth Factor (VEGF)
Cytochrome P450 1A2 (CYP1A2) Genotyping
Selenium, Random, Urine
1,3-Beta-D-Glucan (Fungitell® ß-D Glucan), Bronchial Wash
Amphetamine, Serum
PM-1 (PM-Scl) Antibody
Fibroblast Growth Factor 23 (FGF23), Plasma
LDS
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Alpha Fetoprotein (AFP), Body Fluid
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Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
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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
Alpha Fetoprotein (AFP), Body Fluid
Medical Test
Overview
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