NEOTEC 2008 Call. CDTI6
It is the first project developed by NIMGenetics after its creation, and is focused on prenatal diagnosis by using array CGH technology. The development of the project enabled the market launch of KaryoNIM® Prenatal, capable of detecting, at that time, the 90 main foetal chromosomopathies in a single genetic test. The initial concept has been substantially improved until reaching the design we currently offer, capable of detecting up to 124 genetic syndromes associated with intellectual disability and congenital alterations.