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Showing search results for "algorithm" 61-70 of 301

  1. Cystic Fibrosis Screen

    General screen for carrier status and assessment of CF risk. This test will identify approximately 90% of Cystic Fibrosis (CF) mutations in the Caucasian population, and 97% in the Ashkenazi Jewish population.... More

  2. CEA with HAMA Treatment

    CEA is a tumor marker that is useful to monitor patients with persistent, recurrent or metastatic colonic carcinoma. Patients who have received mouse monoclonal antibodies as part of treatment should have their …... More

  3. Cystic Fibrosis Rare Mutation Analysis, One Exon

    This test is offered to individuals to: 1) detect a known familial CF mutation which is not examined in population-based CF carrier screening assay in at-risk individuals; 2) provide prenatal detection of a known …... More

  4. Chromosomal Microarray, Prenatal, ClariSure Oligo-SNP

    This assay may be useful for: Further investigation on fetuses with abnormal ultrasound findings indicating congenital malformation. Further definition of an imbalanced cytogenetic abnormality. Further …... More

  5. C-Reactive Protein (CRP)

    Increased CRP levels are found in inflammatory conditions including: bacterial infection, rheumatic fever, active arthritis, myocardial infarction, malignancies and in the post-operative state. This test cannot detect …... More

  6. Cardio IQ CYP2C19 Genotype

    This test detects variants in the CYP2C19 gene leading to altered enzyme activity and may require alternative treatments or altered drug dosage of a drug metabolized by CYP2C19 for optimal therapeutic response.... More

  7. CBC (includes Differential and Platelets)

    Basic Test... More

  8. Cystic Fibrosis Gene Deletion or Duplication

    This test detects large deletion or duplication mutations in the CF gene in CF patients or patients with potential diagnosis of CF where only one or no mutation has been identified.... More

  9. CAH (21-Hydroxylase Deficiency) Rare Mutations

    This DNA sequencing test identifies rare mutations in the 21-hydroxylase gene known to cause congenital adrenal hyperplasia (CAH). It is used when individuals are known or suspected to have 21-ohd mutations undetectable…... More

  10. Cardio IQ ASCVD Risk Panel with Score

    This panel provides the 10-year and lifetime risk of atherosclerotic cardiovascular disease (ASCVD) using lipid results with anthropomorphic data and family history. The ASCVD risk assessment is recommended in the 2013…... More

* The tests listed by specialist are a select group of tests offered. For a complete list of Quest Diagnostics tests, please refer to our Directory of Services.