Also Known as
Von Willebrand Disease, VWF
This sequence analysis of exons 1-52 (test code 1395) is optimizedfor detection of germline variants associated with von Willebrand disease (VWD). VWF analysis is appropriate for all types of VWD.
Additional Test Information
Fetal: Amniotic Fluid, CVS, Cultured Amniocytes or Cultured CVS; Parental/Patient: EDTA Whole Blood (lavender top)
Fetal: 7-15 ml Amniotic Fluid or 5-10 mg CVS, backup culture of Amniocytes or CVS is highly recommended; Two T25 flasks Cultured Amniocytes or CVS (2x10^6 minimum); Parental/Patient: 3-5 ml
Fetal: Call Laboratory; Parental/Patient: 2 ml
PCR and Bi-directional DNA Sequencing