Muscular Dystrophies Gene Mutation Panel, NGS
Dopamine beta-hydroxylase (DBH) Genetic Variations
Homovanillic Acid (HVA), Random, Urine
Mucopolysaccharidosis type III
Macroamylase
Galactose-1-Phosphate Uridyltransferase, Blood
Hepatitis C Virus (HCV) Genotyping
Noonan syndrome
MYH7 Gene Mutation Analysis
Chromogranin A
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FLT3 (FMS-related Tyrosine Kinase 3) Mutation Analysis, Blood
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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
FLT3 (FMS-related Tyrosine Kinase 3) Mutation Analysis, Blood
Medical Test
Methodology
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FLT3 (FMS-related Tyrosine Kinase 3) Mutation Analysis, Blood
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