Wolf-Hirschhorn Syndrome, 4p16.3 Deletion
Hereditary Hemorrhagic Telangiectasia, ACVRL1 Gene Mutation Analysis
FLT3 (FMS-related Tyrosine Kinase 3) Mutation Analysis, Blood
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
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Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References
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