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Showing search results for "algorithm" 51-60 of 313
- XSense, Fragile X with Reflex
Fragile X syndrome (FXS OMIM # 300624) is the most common inherited mental retardation syndrome, affecting approximately 1:4000 males and approximately 1:8000 females. The disease is caused by the expansion of a …... More
- XSense, Fragile X with Reflex and Chromosome Analysis, Blood
XSense , Fragile X with Reflex and Chromosome Analysis, Blood CPT Code(s) 88230, 88262, 81243 Includes If Fragile X, PCR result is not Normal, or Gray zone, then Fragile X Methylation Analysis will be performed at an …... More
- von Willebrand Antigen, Multimeric Analysis
For the analysis of von Willebrand antigen multimers for the diagnosis of von Willebrands Disease. Positive results will report out as type 1, type 2, or type 3 along with a narrative comment describing the gel.... More
- von Willebrand Factor Collagen Binding Assay
The Collagen Binding Assay (vWF:CBA) is a test procedure that quantifies the binding of vWF to collagen. Collagen binding of vWF is associated with the functionally more important HMW forms of vWF. Therefore, vWF:CBA …... More
- von Willebrand Comprehensive Panel
von Willebrand Comprehensive Panel CPT Code(s) 85240, 85245, 85246, 85247, 85730 Includes Partial Thromboplastin Time, Activated; Factor VIII Activity, Clotting; von Willebrand Factor Antigen; Ristocetin Cofactor; von …... More
- von Willebrand Factor Antigen
von Willebrand Disease is the most common hereditary bleeding disorder; it may also be acquired. von Willebrand Factor is necessary for platelet adhesion to injured endothelium. von Willebrand Factor Antigen is useful …... More
- T3 Free, Tracer Dialysis
T 3 measurements are used to diagnose hyperthyroidism. This test can also be used to clarify thyroid status in the presence of possible protein-binding abnormalities.... More
- von Willebrand Comprehensive Panel 2
von Willebrand Comprehensive Panel 2 CPT Code(s) 85730, 85240, 85246, 85245, 83520, 85247 Includes Partial Thromboplastin Time, Activated; Factor VIII Activity, Clotting; von Willebrand Factor Antigen; Ristocetin …... More
- von Willebrand Disease (vWD) Type 2N (vWF: Factor VIII Binding Activity)
To differentiate between hemophilia A, hemophilia A carrier state, and type 2N vWD. The Type IIN vWD is assocoated with mild to moderate FVIII deficiency and otherwise normal von Willebrand Antigen and Ristocetin …... More
- Thyroid Cancer Mutation Panel (BRAF, RAS, RET/PTC, PAX8/PPAR)
The thyroid mutation panel assesses for all 8 of the most common mutations or rearrangements associated with thyroid neoplasia. The BRAF codon 600 mutation, and RET/PTC1 and RET/PTC3 rearrangements are highly …... More
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