Acute myeloid leukemia (AML)
Lynch Syndrome Multi Gene Panel (MLH1, MSH2, MSH6, PMS2 and EPCAM), Genomic Unity®
Williams Syndrome, 7q11.23 Deletion, FISH, Blood
Lorazepam, Urine
HIV-1 Integrase Inhibitor Resistance by Sequencing
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NHP2 Gene Mutation Analysis
Eosinophilic esophagitis
Semen Analysis
IMMray, PanCan-d Test for Early Detection of Pancreatic Cancer
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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
Methodology
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von Willebrand Disease 2N (Subtype Normandy), Genotyping
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