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Detects mutations and deletions in the beta-globin (HBB) gene, used to diagnose beta-thalassemia and other hemoglobinopathies.
10,710 THB
Detects mutations in exon 2, 3, and 4 of the MECP2 gene, associated with Rett syndrome, a neurodevelopmental disorder primarily affecting females.
15,390 THB
Identifies genetic mutations and inheritance patterns in embryos before implantation, used for families with a known risk of monogenic diseases.
365,781 THB
Whole genome sequencing to detect genetic mutations and variations across the entire genome.
103,500 THB