VWD Type 2N Sequence Analysis
Order Code: 1288 Get Requisition Form
Sequence analysis of VWF exons 17-21 and 24-27 detects germline variants associated with type 2N von willebrand disease (VWD).
Also Known As
- Von Willebrand Disease
von Willebrand Disease
EDTA Whole Blood, EDTA Bone Marrow, DNA, Buccal Swabs, Amniotic Fluid, Cultured Amniocytes, Direct or Cultured CVS, ACDA Whole Blood, ACDB Whole Blood, Na Heparin Whole Blood
3-5 mL EDTA Whole Blood or Bone Marrow (lavender top), 3-4 Buccal Swabs, >=1 ug DNA at >=50 ng/uL, 7-15 mL Amniotic Fluid, 5-10 mg CVS, 2-T25 flasks cultured amniocytes or CVS (2x10^6 minimum)
Minimum / Pediatric Volume
Fetal: Call Laboratory; Parental/Patient: 2 mL EDTA whole blood
Room Temperature or Refrigerated
Capture Hybridization and Next Generation Sequencing with supplementary PCR and bi-directional Sanger sequencing for quality and coverage.
New York State Approval
Yes, visit app.dexzcodes.com