Nickel, Random, Urine
Amitriptyline, Urine
CPM, 12q15, for Well-Differentiated Liposarcoma/Atypical Lipomatous Tumor, FISH
Histoplasma capsulatum Antibody, CSF
Methlyenetetrahydrofolate reductase (MTHFR) Mutation Analysis
Alpha 1 Antitrypsin Genotyping/Phenotyping
Glucose, Random, Blood
Kallmann Syndrome, Xp22.3 Deletion, FISH
Fine Needle Aspiration Biopsy and Fine Needle Core Biopsy
Macroprolactin, Serum

LDS
Sign up
Log in

LDS
/Medical Tests
/von Willebrand Disease 2N (Subtype Normandy), Genotyping

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

von Willebrand Disease 2N (Subtype Normandy), Genotyping
Medical Test

Access to von Willebrand Disease 2N (Subtype Normandy), Genotyping is restricted.