Amyloid Protein Identification
ASXL1 Gene Mutation Analysis
Lactoferrin, Fecal
RET Gene Rearrangements by FISH
MLH1 Hypermethylation (Promoter Methylation) Analysis, Tissue
Toxoplasma gondii, Molecular Detection, PCR
Anthrax DNA by Molecular Method
Fibrinogen (Functional)
FibroTest (FibroSURE), Liver Fibrosis Test
AFF2 (AF4/FMR2 family, member 2) Gene Mutation Analysis
LDS
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Kallmann Syndrome, Xp22.3 Deletion, FISH
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
Kallmann Syndrome, Xp22.3 Deletion, FISH
Medical Test
References
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Kallmann Syndrome, Xp22.3 Deletion, FISH
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