CFTR (whole gene NGS)
Phenylketonuria, Phenylalanine Hydroxylase Deficiency PAH
GeneScreen® Standard
GeneScreen® is a carrier screening test that allows you to perform a multiple analysis of hereditary genetic disorders. The GeneScreen® Standard test includes the most common and clinically relevant pathologies, including disorders specific for individuals of Ashkenazi Jewish descent (550+ genes, 700+ genetic disorders).
GeneScreen® Easy
GeneScreen® Focus
PrenatalScreen® Standard
The PrenatalScreen® Standard test includes the analysis of a wide number of genes and the most common and clinically relevant diseases (740+ genes, 1000+ genetic conditions).
GeneSafe Inherited®
GeneSafe® De Novo
PrenatalSafe® 5
PrenatalSafe® is a non-invasive prenatal test that detects chromosomal abnormalities by analyzing cell-free fetal DNA from a pregnant woman’s blood sample. The PrenatalSafe® 5 test detects aneuploidies of chromosomes 21, 18, 13 and sex chromosomes (X and Y), as well as including fetal sex determination (optional). PrenatalSafe® 5 is not indicated or dichorionic twin pregnancies. […]
