Newborn screening tests look for developmental, genetic, and metabolic disorders in the newborn baby
More InformationUrine organic acids is a medical diagnostic test that measures organic acid metabolites in the urine.
More InformationChromosomal Microarray (CMA) is a microchip-based testing platform that allows automated analysis of many pieces of DNA at once
More Informationall the exons in a genome are known as the exome, and the method of sequencing them is known as whole exome sequencing.
More InformationPlasma Amino Acid test is done postnatally, to look for the uncontrolled amount of amino acids in the blood and is a screening test.
More InformationThe maternal serum screening test is a blood test offered to pregnant women.
More InformationNIPT test is able to detect small fragments of DNA from the baby, in the mother's blood.
More InformationFISH is a rapid test of the numbers of selected chromosomesn in a blood sample, a sample of the placenta, CVS, amniotic fluid, or fetal blood.
More Information(QF-PCR) is a molecular- based technique employed for prenatal and postnatal diagnosis of rapid aneuploidy detection(RAD) of chromosomes 13, 18, 21, X, and Y.
More InformationChromosomal Microarray (CMA) is a microchip- based testing platform that allows automated analysis of many pieces of DNA at once
More Informationkaryotype test looks at the size, shape, and number of your chromosomes. Chromosomes are the parts of your cells that contain your genes.
More InformationSanger sequencing is a robust testing strategy able to determine whether a point mutation or small deletion/duplication is present.
More InformationCouple Screen ideal for preconception screening, to determine the carrier status of common genetic disorders in the couple to estimate the risk of passing on a genetic disorder to their future offspring.
More InformationPreimplantation genetic testing comprises a group of genetic assays used to evaluate embryos before transfer to the uterus.
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