P scanning / Pre-implantation Genetic Screening
MGMED is currently offering a service to select superior embryos before In Vitro Fertilization-Pre-Embryo Transfer (IVF-ET) for minimizing risks of congenital birth defects and increasing pregnancy success rate.
N scanning / Non-invasive prenatal Screening
N scanning is a non-invasive screening method using cell-free fetal DNA in maternal blood to detect fetus’s chromosomal abnormalities.
G scanning / Post-natal Genetic Screening
G-scanning is a newborn genetic screening method using newborn’s DNA in the blood to detect chromosomal abnormalities.
M scanning / Pre-natal Genetic Screening
M-scanning is a prenatal genetic screening method using fetal DNA in chorionic villus to detect chromosomal abnormalities.
S scanning / Stem-cell Genetic Screening
S-scanning is a screening service using DNA-chip for the chromosomal abnormalities in stem cells.
C scanning / Cancer-cell Genetic Screening
C-scanning is a screening service to confirm the unique chromosomal patterns of cancer cells to check the recurrence of cancer.