Immune Complex Panel
Carnitine, Total, Urine
Rare Constitutional and hereditary Diseases, Whole Exome Sequence Analysis, NGS
15q Deletion, Type I and Type II Characterization, Prader-Willi/Angelman Syndromes, FISH
21-Hydroxylase Antibody
Leptin
Hydroxyzine, Serum
17-Ketosteroids, Urine
Cryptococcus Antigen, Serum
Fluoxetine, Serum
LDS
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TNNI3 (Troponin I) Gene Mutation Analysis
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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
TNNI3 (Troponin I) Gene Mutation Analysis
Medical Test
Turnaround Time
Access to
TNNI3 (Troponin I) Gene Mutation Analysis
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