I have a question regarding whole genome testing for my son and I.
My son and I both share an immune deficiency that is of yet unsolved. We get infections and don’t create an elevated wcb or it’s a delayed wcb, and it would be great if I could get both of our entire genome sequenced, so we can start by looking at the mutations we share in common.
Is there a way to get an exception for the under 18 rule? Especially since this for his benefit, as much as it is for mine.
Thank for your help.