Test Code: PNL135

Genes: ACVR2B, CFC1, CRELD1, GJA1, GDF1, FOXH1, LEFTY2, MMP21, NKX2-5, NODAL, ZIC3 (11 genes)

Sample Type: 3 ml peripheral blood in EDTA (purple/pink top) tube

Method:

Turnaround Time: 3 weeks

Courier: Ship overnight at room temperature to receive next day. Do not refrigerate or freeze. Maintain specimen at room temperature.

Price: 1800

Description:
Heterotaxy syndrome, Tetralogy of Fallot, and VACTERL/VATER associations are congenital conditions that often co-occur or share overlapping features involving multiple organ systems, especially the heart, gastrointestinal tract, and limbs.