Copper, Liver Tissue
Peripheral Myelin Protein 22 (PMP22) Gene Mutation Analysis
Coenzyme Q10, Reduced and Total, Plasma
Elastase, Pancreatic, Serum
Ceramide Trihexosides and Sulfatides, Urine
Maternal Serum Screen, Alpha Fetoprotein (AFP) for Neural Tube Defect
Williams Syndrome, 7q11.23 Deletion, FISH, Blood
Inhibin B
Barrett's-Associated Neoplasia, Cytology
Cortisol, Salivary
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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Clinical Utility
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Genetic Testing for Severe Inherited Diseases, NGS
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