Carnitine, Total, Urine
Salivary Gland Tumor, MYB (6q23) Rearrangement by FISH
Chromosome Analysis, Body Fluid
21-Hydroxylase Antibody
Coxsackie A Virus Antibodies, CSF
Cytochrome P450 1A2 (CYP1A2) Genotyping
Selenium, Random, Urine
Complement Component C3, Nephritic Factor
Gram Stain, Routine
Legionella pneumophila Antibody, IgM by IFA
LDS
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Rare Constitutional and hereditary Diseases, Whole Exome Sequence Analysis, NGS
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References
All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References
Rare Constitutional and hereditary Diseases, Whole Exome Sequence Analysis, NGS
Medical Test
References
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Rare Constitutional and hereditary Diseases, Whole Exome Sequence Analysis, NGS
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