Arrhythmogenic Cardiomyopathy Gene Mutation Panel, NGS
1p36 deletion (monosomy) syndrome
Interleukin 6 (IL-6), Serum
Haptoglobin
Acetoacetate (Ketones), Urine
Culture, Acid-Fast Bacilli, Sputum
Protein S, Functional
Anticholinergic poisoning
Chymotrypsin, Stool
HER2/neu (ERBB2) Gene Amplification, FISH, Urothelial Carcinoma
LDS
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Primary Hyperoxaluria Gene Mutation Panel
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
Primary Hyperoxaluria Gene Mutation Panel
Medical Test
CPT
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Primary Hyperoxaluria Gene Mutation Panel
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