Carnitine Palmitoyltransferase II Deficiency, Gene Mutation Analysis
Pregnenolone
Fibroblast Growth Factor Receptor 3 (FGFR3) Mutation Analysis in Bladder Cancer
Kallmann Syndrome, Xp22.3 Deletion, FISH
Adenovirus Antigen Detection
Human Chorionic Gonadotropin (hCG), Qualitative, Urine
Reticulocyte Count
Comprehensive Mitochondrial Disorders Gene Analysis Panel, NGS (Genomic Unity®)
Amyloid Protein Identification
GRACILE Syndrome
LDS
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von Willebrand Factor Multimer Analysis, Plasma
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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
von Willebrand Factor Multimer Analysis, Plasma
Medical Test
Specimen Collection
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von Willebrand Factor Multimer Analysis, Plasma
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