CeGaT’s Prenatal Diagnostics portfolio supports genetic questions before birth with both invasive and non-invasive testing options. Depending on the indication, physicians can request Prenatal ExomeXtra®, prenatal array CGH, prenatal single gene and segregation analysis, the Harmony® Test or Rhesus-NIPT. These services can help clarify suspicious ultrasound findings, familial hereditary diseases, chromosomal abnormalities or fetal Rh factor status. CeGaT uses modern sequencing technologies, microarrays and MLPA examinations where appropriate. The aim is to provide reliable genetic information during pregnancy, supporting physicians and families with medically relevant results while choosing the most suitable test according to the clinical question and sample type.