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Showing search results for "algorithm" 61-70 of 314
Calcitonin concentration is increased in patients with medullary thyroid carcinoma. Calcitonin concentrations may be used to monitor disease.... More
- Chromosome Analysis, Hematologic Malignancy
Cytogenetics of hematologic disorders attempts to define and interpret chromosomal aberrations that occur in neoplastic cells associated with leukemia, lymphoma and other hematologic malignancies. Chromosome …... More
- CAH (21-Hydroxylase Deficiency) Common Mutations
This test identifies mutations in the 21-hydroxylase gene known to cause congenital adrenal hyperplasia (CAH). It is used to: 1) confirm or establish a diagnosis of CAH due to 21-OH deficiency; 2) identify genetic …... More
- Childhood Allergy (Food and Environmental) Profile: Puerto Rico
Childhood Allergy (Food and Environmental) Profile: Puerto Rico CPT Code(s) 82785, 86003 (x12) Includes IgE allergy testing for: Alternaria alternata (m6) Cat Dander (e1) Cockroach (i6) Corn (f8) Cow's Milk (f2) …... More
- c-KIT Mutation Analysis, Cell Based
Activating c-KIT mutations have been indentified in various human cancers. c-KIT exon 8 and 17 mutations have been described in patients with CBF-AMLs and usually confer a poor prognosis with increased relapse rate. c-…... More
- Calprotectin, Stool
Used to diagnose inflammatory bowel disease (IBD), including Chron's disease and ulcerative colitis, or to differentiate IBD from irritable bowel syndrome (IBS).... More
- Carnitine, LC/MS/MS
Serum carnitine analysis is useful in the diagnosis and monitoring of patients with carnitine deficiency (either primary or secondary). Primary carnitine deficiency is an autosomal recessively inherited genetic …... More
- Chromosome Analysis, CLL/LPD
Chromosome Analysis, CLL/LPD CPT Code(s) 88237, 88264 Methodology Culture Karyotype Reference Range(s) See Laboratory Report... More
- Chromosome Analysis, Lymph Node
For diagnosis and prognosis of hematologic malignancies, specific to a tumor site.... More
- Chromosomal Microarray, Postnatal, ClariSure Oligo-SNP
Determine genetic cause of Developmental Delay (DD) or Mental Retardation (MR) in patients with or without dysmorphic features. Confirm, exclude, (or clarify) the diagnosis of known chromosomal syndromes. Assist in …... More
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