Prenatal diagnosis
Microgenomics Laboratory offers services of prenatal diagnosis using the array-CGH technique.
Array-CGH analysis in prenatal period can detect possible genomic alterations in a fetus. The test uses DNA obtained from amniotic fluid or CVS to investigate the whole genome in a single test.
Below we provide a detailed brochure about the use of molecular karyotype in prenatal period.
Molecular investigations, CGH-Array, Brochure, Molecular karyotype, Prenatal diagnosis