Comprehensive Epilepsy Gene Mutation Panel, NGS
CHIC2, 4q12 Deletion (FIP1L1 and PDGFRA Fusion), FISH, Blood
Hyperthyroidism and other causes of thyrotoxicosis
Helicobacter pylori gastrointestinal tract infection
Beckwith-Wiedemann Syndrome (BWS)/Russell-Silver Syndrome (RSS) Molecular Analysis
Hereditary diffuse gastric cancer
Lecithin-sphingomyelin (L/S) Ratio
Ganciclovir, Serum
Viral hepatitis
Calcium, Random, Urine
LDS
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TNNI3 (Troponin I) Gene Mutation Analysis
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
TNNI3 (Troponin I) Gene Mutation Analysis
Medical Test
Overview
Access to
TNNI3 (Troponin I) Gene Mutation Analysis
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