Baby Gender test is used alongside in-vitro fertilization (IVF) to screen 5 most common abnormalities in embryos that is chromosome 21, 18, 13, X and Y.
The abnormalities are identified as chromosome 21 – Down Syndrome, 18 – Edwards Syndrome, 13 – Patau Syndrome.
The information obtained also provides the details of the gender of the embryo prior to transfer to help couples fulfil their family planning desires
It is indicated for couples who want to have a baby of a particular gender
What is the procedure?
