Pentobarbital, Urine
Brugada Syndrome Multi-Gene Panel, NGS
Babesia microti Antibody, IgM, IFA
Phosphorus (Phosphate), Serum
Phenylephrine, Urine
Cohen Syndrome Mutation Genetic Analysis
Kallmann Syndrome, Xp22.3 Deletion, FISH
Carcinoembryonic Antigen (CEA), Serum
MSH2 Gene Mutation Analysis (Known Mutations, Duplication/Deletion/Sequencing)
Blastomyces Antibody, Serum

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/Oncology Pharmacogenetics (PGx) Gene Variation Panel

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

Oncology Pharmacogenetics (PGx) Gene Variation Panel
Medical Test

Access to Oncology Pharmacogenetics (PGx) Gene Variation Panel is restricted.