Karyotyping is the quintessential test in the diagnosis of genetic diseases/disorders related to numerical or structural changes of chromosomes. It is crucial to identify prenatal malformation syndromes and recurrence risk for future pregnancies as well as postnatal abnormalities through cytogenetic investigations. The cytogenetic analysis is predominantly carried out using samples - prenatal (Chorionic villus sampling, Amniotic fluid and Cord blood), postnatal samples (Bone marrow, Peripheral blood) and Products of conception. Nowadays, the samples are cultured and processed for analysis in wellequipped laboratories with computerized karyotyping workstations and is currently being used for identification and detection of genetic diseases. The objective of this workshop is to provide hands on training and basic understanding of karyotypes and their interpretation for clinical applications.
Download Registration Form: Click Here
More Details: Click Here