Salivary Gland Tumor, MYB (6q23) Rearrangement by FISH
Duodenal Mucosal Biopsy, Endoscopic
15q Deletion, Type I and Type II Characterization, Prader-Willi/Angelman Syndromes, FISH
Long QT Syndrome Multi-Gene Panel, NGS
Prostaglandin D2 (PGD2), Serum
Vitamin A
Propoxyphene, Confirmation, Urine
Interleukin 6 (IL-6), Serum
Endomysial (EMA) Antibody, IgG and IgM
Histoplasma Antigen, CSF
LDS
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Hereditary Hemorrhagic Telangiectasia, ENG Gene Mutation Analysis
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
Hereditary Hemorrhagic Telangiectasia, ENG Gene Mutation Analysis
Medical Test
Clinical Utility
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Hereditary Hemorrhagic Telangiectasia, ENG Gene Mutation Analysis
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