CarioChip® is a diagnostic tool to analyze human genome to identify large or small chromosomal abnormalities causing congenital or hereditary malformations and/or intellectual disabilities. The DNA of fetal cells or blood of a person is hybridized on a genomic microchip to identify them.
Benefits over conventional techniques:
Results in one week (depending on sample type and volume).
2. More resolution
Identifies small genetic alterations undetectable by conventional karyotyping.
3. Higher capacity
Diagnostic interpretation (allows the identification of more than 250 syndromes).
Turnaround time: 6 working days (monday to friday) (depending on sample volume)
Turnaround time: 15 working days (monday to friday) (depending on sample volume)