Chromosomal studies to identify aneuploidies (extra or missing chromosomes), translocations and balanced rearrangements.
For rapid detection of common aneuploidies (extra of missing chromosomes).
Chromosomal Microarray Analysis (CMA)
For detection of micro-deletion/duplications across the genome in addition to aneuploidies.
Detecting mutations and specific genetic disorders (e.g Thalassemia, Noonan Syndrome etc).