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
Sulfamethoxazole, Serum
Acetylcholinesterase (AChE), Blood

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LDS
/Medical Tests
/Brugada Syndrome Multi-Gene Panel, NGS

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

Brugada Syndrome Multi-Gene Panel, NGS
Medical Test

Access to Brugada Syndrome Multi-Gene Panel, NGS is restricted.