Bacterial Culture, Blood
Myosin regulatory light chain 2 (MYL2) Gene Mutation Analysis
UBE3A Gene Mutation Analysis, Angelman Syndrome, Blood
5-Methyltetrahydrofolate
Giardia lamblia Antibody, IgG, IgA, IgM, IFA
Trisomy 13 (Patau syndrome)
Anchovy, IgE
Cystic Fibrosis (CFTR) Gene Mutation Analysis
Hematocrit/Microhematocrit
HLA-B27 Genotyping, Ankylosing Spondylitis

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/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.