Factor XIII (F13A1) V34L Genetic Variation Analysis
X and Y Aneuploidy Detection, FISH
CHEK2 Gene Mutation Analysis
Transferrin Receptor, Soluble
Biopsy, Blood Vessel
Ethosuximide, Urine
Coccidioides Antibody, IgG and IgM
15q Deletion, Type I and Type II Characterization, Prader-Willi/Angelman Syndromes, FISH
Morphine, Urine
Krabbe Disease (GALC) Gene Mutation Analysis
LDS
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Spondylosis and associated disorders
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SNOMED
Spondylosis and associated disorders
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SNOMED
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