von Willebrand Disease 2N (Subtype Normandy), Genotyping
Acute myeloid leukemia (AML)
Lynch Syndrome Multi Gene Panel (MLH1, MSH2, MSH6, PMS2 and EPCAM), Genomic Unity®
Williams Syndrome, 7q11.23 Deletion, FISH, Blood
Lorazepam, Urine
HIV-1 Integrase Inhibitor Resistance by Sequencing
Bacterial vaginosis
NHP2 Gene Mutation Analysis
Eosinophilic esophagitis
Semen Analysis
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Croup
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Croup
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Medical Tests (11)
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Croup
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ICD10
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Croup
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Additional ICD10
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Croup
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SNOMED
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Croup
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