Newborn genetic screening

Catalog of tests

CEN4GEN offers several innovative testing options for supplemental newborn screens, and these include:

CEN4GEN supplemental newborn exome screen

The CEN4GEN supplemental newborn exome screen is a cutting edge comprehensive screen of more than 22000 genes. Especially clinically useful for screening a wide spectrum of genetic disorders which are treatable when detected early, to complement biochemical genetic testing. This test is also recommended and extremely informative for the clinical diagnosis of newborns with other clinical conditions which have a genetic basis, and for those newborns who are clinically symptomatic. Contact CEN4GEN for more information.

CEN4GEN supplemental newborn mitochondrial genome screen

The CEN4GEN supplemental newborn mitochondrial screen is a cutting edge comprehensive screen of the mitochondrial genome to complement biochemical genetic testing. This test is also extremely informative for the clinical diagnosis of newborns with other clinical conditions which have a genetic basis, and for those newborns who are clinically symptomatic. Contact CEN4GEN for more information.

CEN4GEN supplemental newborn whole genome screen

The CEN4GEN supplemental newborn genome screen; a cutting edge comprehensive screen of the whole genome. Especially clinically useful for screening a wide spectrum of genetic disorders which are treatable when detected early, to complement biochemical genetic testing. This test is also recommended and extremely informative for the clinical diagnosis of newborns with other clinical conditions which have a genetic basis, and for those newborns who are clinically symptomatic. Contact CEN4GEN for more information.