Multiple endocrine neoplasia, type II
Usher Syndrome, Types 1F and 3 (PCDH15 and CLRN1), 2 Variants
Hereditary Hemorrhagic Telangiectasia, ACVRL1 Gene Mutation Analysis
Methaqualone, Urine
Coagulation Factor V Activity Assay, Plasma
HER2/neu (ERBB2), IHC, Semi-Quantitative, Other Tissue
Spinobulbar Muscular Atrophy (Kennedy Disease), Androgen Receptor Gene Mutation Analysis
Ferritin
Bone Morphogenetic Protein Receptor Type II (BMPR2) Gene Mutation Analysis
ATN1 (Atrophin 1) Gene Mutation Analysis
LDS
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Giardia lamblia Antibody, IgG
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
Giardia lamblia Antibody, IgG
Medical Test
Additional Testing
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Giardia lamblia Antibody, IgG
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