My wife and I just birthed a baby girl. About two weeks after delivery we were told that she has a chromosome deficiency, i.e., Chromosome 22.q.11 Duplication Syndrome. This lead to heart disease at birth. We banked her cord blood before this was discovered. My question now is what if any future application the cord blood may have for her, family members, etc., given the chromosome deficiency that is likely within the cord blood?