Also Known as
Von Willebrand Disease, VWF
This assay is designed for detection of the D1472H polymorphism within the VWF gene.
Additional Test Information
Amniotic Fluid, Buccal Swabs, Cultured Amniocytes, CVS, DNA, EDTA Bone Marrow, EDTA Whole Blood
Additional Sample Requirements
Sample should be less than 7 days old when received in the laboratory.
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)
PCR and Bi-directional DNA Sequencing