With today’s technology it is much easier to test a baby’s chromosomes. After giving birth, chromosome analysis can be done via blood test, before birth via prenatal testing i.e. Amniocenteses or Chorionic villus sampling. This topic is controversial and there are mixed feelings if the testing should be done. I feel that doing prenatal testing in advance is unnecessary because generally, people do not terminate a pregnancy even when they hear that the fetus might have chromosomal abnormalities. Why should one go through all the angst of taking the controversial test and then wait with fear for the results? And even when one hears bad news, there is always that small percent chance that the results are wrong.
There are two different chromosomal
There are two different chromosomal