CNBP Genetic Analysis for Myotonic Dystrophy, Type II (DM2)
Hereditary Hemorrhagic Telangiectasia, Gene Mutation Panel
Bartonella Antibody, IgG, Serum
ADAMTS13 Activity and Inhibitor Assay
Megaloblastic anemia (Myelodysplastic syndrome)
Aldosterone, 24 Hour, Urine
Beta-Glucuronidase, Fibroblasts
Bruton Tyrosine Kinase (BTK) Protein Expression by Flow Cytometry
Cytochrome P450 1A2 (CYP1A2) Genotyping
Aspergillus (Galactomannan) Antigen, Serum
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Lymphadenopathy
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Lymphadenopathy
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SNOMED
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