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Showing search results for "thyroid cancer" 51-60 of 246

  1. Microsatellite Instability (MSI), HNPCC

    Patients with early onset and family history of colon cancers are suggestive of Hereditary Nonpolyposis Colon Cancer (HNPCC) syndrome. Microsatellite instability analysis on tumor tissue is recommended as a screening …... More

  2. MUTYH Sequencing and Deletion/Duplication

    Mutations in MUTYH are causative of MUTYH-associated polyposis (MAP). Unlike many of the hereditary cancer conditions, MAP is a recessive condition. Individuals with MAP have an increased lifetime risk of polyposis and …... More

  3. Juvenile Polyposis Panel (BMPR1A and SMAD4)

    Mutations in BMPR1A and SMAD4 are associated with Juvenile Polyposis syndrome (JPS). Individuals with JPS, have an increased risk for colorectal cancer (40-50%) and gastric cancer (up to 21%, if multiple polyps are …... More

  4. {"col2": 14-3-3 Protein, CSF p53 Oncoprotein with Interpretation p53 Oncoprotein, IHC without Interpretation Pain Management Base Profile with Confirmation, Urine Pain Management Base Profile with Confirmation, …... More

  5. CellSearch Circulating Tumor Cells, Breast

    This test can detect the presence of Circulating Tumor Cells (CTC) in the peripheral blood of metastatic breast cancer, colorectal or prostate cancer in patients. A count of CTC of 5 or more in breast and prostate …... More

  6. Lynch Syndrome, MLH1 Sequencing and Deletion/Duplication

    Sequencing: This test should be offered to patients with colorectal cancer who meet the Bethesda criteria established by the National Cancer Institute (NCI), and/or that their tumors display microsatellite instability (…... More

  7. Lynch Syndrome, MSH6 Sequencing and Deletion/Duplication

    Sequencing: This test should be offered to patients with colorectal cancer who meet the Bethesda criteria established by the National Cancer Institute (NCI), and/or that their tumors display microsatellite instability (…... More

  8. Lynch Syndrome, MSH2 Sequencing and Deletion/Duplication (Including EPCAM)

    Sequencing: This test should be offered to patients with colorectal cancer who meet the Bethesda criteria established by the National Cancer Institute (NCI), and/or that their tumors display microsatellite instability (…... More

  9. TP53 Somatic Mutation, Prognostic

    Somatic mutation of the p53 tumor suppressor gene is the most common genetic alteration seen in human cancers, with 50% of adult human tumors bearing inactivating mutations or insertions, deletions in the P53 gene. …... More

  10. STK11 Sequencing and Deletion/Duplication

    Mutations in the STK11 (aka LKB1) gene causes Peutz-Jeghers syndrome (PJS) which is an autosomal dominant disorder with an increased risk of various neoplasms (especially gastrointestinal and breast cancers). Sequencing…... 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.