Autoinflammatory Syndromes (VEXAS syndrome)
BCR-ABL, Translocation, FISH, Blood
Giardia lamblia Antibody, IgG
Multiple endocrine neoplasia, type II
Usher Syndrome, Types 1F and 3 (PCDH15 and CLRN1), 2 Variants
Hereditary Hemorrhagic Telangiectasia, ACVRL1 Gene Mutation Analysis
Methaqualone, Urine
Coagulation Factor V Activity Assay, Plasma
HER2/neu (ERBB2), IHC, Semi-Quantitative, Other Tissue
Spinobulbar Muscular Atrophy (Kennedy Disease), Androgen Receptor Gene Mutation Analysis
LDS
Sign up
Log in
LDS
/
Medical Tests
/
Factor XIII (F13A1) V34L Genetic Variation Analysis
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
Factor XIII (F13A1) V34L Genetic Variation Analysis
Medical Test
Methodology
Access to
Factor XIII (F13A1) V34L Genetic Variation Analysis
is restricted.
Sign up now