I think that is might be the last one, I'm not all that sure though
If the mother is a carrier and the father is normal, the outcomes for potential children would be:
XH Xh
XH XHXH XHXh
Y XHY XhY
So let’s break these down
XHXH = will be a daughter (XX) with normal blood (HH)
XHXh = will be a daughter (XX) who is a carrier for hemophilia (Hh)
XHY = will be a son (XY) with normal blood (H)
XhY = will be a son (XY) with hemophilia (h)
Because this disease is inherited on the X chromosome, male offspring tend to either have it or not. They can’t be carriers because they only have one X chromosome. So the chances of having a son with hemophilia will be 50% cause the boys have a 50% chance of inheriting hemophilia.
On the other hand, daughters will either have normal blood or be carriers in this situation. So to answer the question, the chance a daughter of this couple would have of inheriting hemophilia is 0%. This only changes if their father has hemophilia. Then they will either be a carrier or will have hemophilia.
Noun, Genetics. 1. the principle, originated by Gregor Mendel, stating that during the production of gametes the two copies of each hereditary factor segregate<span> so that offspring acquire one factor from each parent. Expand. Also called Mendel's first law, Mendel's law.</span>
Answer:
G1 Checkpoint
Explanation:
Data indicates that the G1 checkpoint is activated in response to mitotic DNA damage in the presence of p53, and that the mitotic DNA damage response is connected to the G1 checkpoint by p53. If cells continue to possess damaged DNA, apoptosis is induced in a p53-dependent manner.
The fact that the new born's organs aren't mature enough to eliminate all the billirubin and an imbalance between the production and the elimination of the bilirubin occurs!