Williams Syndrome, 7q11.23 Deletion, FISH, Tissue
Immunoglobulin M (IgM), Serum
EsoGuard Methylation Assay for Barrett’s Esophagus
Mycoplasma pneumoniae, Culture
Estrogen/Progesterone Receptor, IHC
HLA C Genotype
Lamotrigine, Urine
JAK2 (V617F) Gene Mutation Analysis
PML-RARA (Promyelocytic Leukemia/Retinoic Acid Receptor Alpha) Translocation, t(15;17) Analysis
Diabetic nephropathy
LDS
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JAK2 (V617F) Gene Mutation Analysis
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Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
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All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References
JAK2 (V617F) Gene Mutation Analysis
Medical Test
ICD10
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