Williams Syndrome, 7q11.23 Deletion, FISH, Tissue
Methylphenidate, Urine
Hereditary Hemolytic Anemia Gene Mutation Panel, NGS
Gastrointestinal Stromal Tumor Gene Mutation Panel, NGS
Ethanol (Alcohol), Urine
Soluble Fibrin Monomer
Treponema pallidum Antibody, FTA-ABS, IgG, CSF
Polyoma BK Virus, PCR, Plasma
Diphenhydramine, Urine
Mantle Cell Lymphoma, bcl-1/JH t(11;14), Real-time PCR, Bone Marrow
LDS
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Pregnenolone
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Diseases
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CPT
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All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
LOINC
ICD10
Additional ICD10
References
Pregnenolone
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Interpretation
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