Test Code: 1P36MD

Genes: (0 genes)

Sample Type: Blood, Amniotic Fluid, Chorionic Villus Sampling

Method: Multiplex Ligation-dependent Probe Amplification (MLPA)

Turnaround Time: 7 Days

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

Price: 1000

Description:
1p36 deletion syndrome is a contiguous gene deletion disorder caused by loss of genetic material at the terminal end of the short arm of chromosome 1 (1p36). MLPA (Multiplex Ligation-dependent Probe Amplification) is a targeted method used to detect such deletions with high resolution.