Cystic Fibrosis, CFTR Gold

Includes the Control of CFTR Cystic Fibrosis, HBB β-Thalassemia, HBA1, HBA2 α-Thalassemia genes, as well as the detection of the SMN1 "2 + 0" genotype (SMN1 silent mutation).

The GOLD IVF package also includes the control of β-thalassemia genes (deletions of HBB & HBD genes), SMN1 Spinal Muscular Atrophy (~ 95%) and the detection of the most common mutation for deafness of the GJB2 gene (35del).

Response Time 2-3 weeks.