Copper, Liver Tissue
HLA-B51 Genotyping for Behçet’s Disease
Haptoglobin Genotyping
Hereditary Neuroendocrine Tumor Gene Mutation Panel, NGS
Vitamin B2 (Riboflavin)
Amino Acids Quantitative by LC-MS/MS, Plasma
Lyme Disease (Borrelia burgdorferi) Antibody, IgG, IgM, Spinal Fluid
Spinocerebellar Ataxia, Ataxin 8 (ATXN8OS) Gene Mutation Analysis
Delayed puberty (male and female)
LDS
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Genetic Testing for Severe Inherited Diseases, NGS
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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
Genetic Testing for Severe Inherited Diseases, NGS
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Additional Testing
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Genetic Testing for Severe Inherited Diseases, NGS
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