Williams Syndrome, 7q11.23 Deletion, FISH, Tissue
Phospholamban (PLN) Gene Mutation Analysis
Myoglobin, Serum
Aluminum, Serum
Dihydropyrimidine Dehydrogenase (DPYD) Genotyping
Clonidine (Catapres), Urine
PM-1 (PM-Scl) Antibody
Legionella Antigen, Urine
Selenium/Creatinine Ratio, Random, Urine
Hereditary Angioedema Diagnostic Panel
LDS
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Familial Hypercholesterolemia and Related Diseases Multi-Gene Panel, NGS
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
Familial Hypercholesterolemia and Related Diseases Multi-Gene Panel, NGS
Medical Test
Clinical Utility
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Familial Hypercholesterolemia and Related Diseases Multi-Gene Panel, NGS
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