GENOMICS HUB GENETIC COUNSELLORS SPECIALTIES

This test is done to confirm a clinical diagnosis or to provide the opportunity to exclude other genetic disorders, thereby narrowing down the possible diagnosis.

This test determines if an adult with or without symptoms, has a genetic mutation that increases their children's chance of inheriting the disorder.

This is a non-diagnostic test aimed to identify infants with certain congenital disorders early on. 

This test is for adults with no symptoms of a specific disorder and is done to determine if they carry a genetic mutation that increases the probability of developing symptoms of the disorder.