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
Coccidioides By Molecular Method, Body Fluid

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/Comprehensive Epilepsy Gene Mutation 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

Comprehensive Epilepsy Gene Mutation Panel, NGS
Medical Test

Access to Comprehensive Epilepsy Gene Mutation Panel, NGS is restricted.