Usher Syndrome, Types 1F and 3 (PCDH15 and CLRN1), 2 Variants
Uric Acid, Body Fluid
Tubulin receptor (Tubulin) Antibody, IgG
Acid Sphingomyelinase Activity
Dopamine receptor 1 (DRD1) Genotyping
Factor XIII (F13A1) V34L Genetic Variation Analysis
MSK-IMPACTâ„¢, Solid Organ Gene Cancer Panel
PML-RARA Translocation, t(15;17) by RT-PCR, Quantitative
Lymphocytic Choriomeningitis (LCM) Virus Antibody, IgG
Celiac Disease, IgG and IgA
LDS
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PPOX Gene Mutation Analysis, Blood
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References
PPOX Gene Mutation Analysis, Blood
Medical Test
Turnaround Time
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PPOX Gene Mutation Analysis, Blood
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