If I were hired as a genetic counselor to advise a couple about the odds of the couple having a baby with a genetic disorder and I wanted to order lab tests to be done on the pregnant mother to determine if the baby has a genetic disorder (amniocentesis)-what kind of test would be done? How would the test determine if the baby has a genetic disorder or not? If it is determined that the couple's baby has a genetic disorder, then what advice should I provide to that couple? Why? What if the couple went against my advice? Whose advice (mine-the genetic counselor representing science or the couple representing society) should be considered?
Answer:thousands of kelvins
Explanation: just got it right on test
Answer:
25% heterozygous tall
Explanation:
If we take the F1 generation as parents and let them self-fertilise, we have 4 crosses.
The first one for homozygous tall, then we have 100% AA.
The second and third one for heterozygous tall and we have 25% AA, 50%Aa and 25%aa for each of them.
The last one would be for dwarf, and we'll have 100%aa.
Adding all of them, we'll have
AA = 100 + 25 + 25 = 150%
Aa = 50+50 = 100%
aa = 100 + 25 + 25 = 150%
as we had 4 crosses, so dividing the total percentages by 4, we'll have,
AA = 37.5%
Aa = 25%
aa = 37.5%
:. The percentage of heterozygous tall would be 25%.
Hope it helps:)
Answer:
Explanation: When the cell increases in size, the volume increases faster than the surface area, because volume is cubed where surface area is squared. When there is more volume and less surface area, diffusion takes longer and is less effective. ... this is actually why cells divide.
Explanation:
Answer: 3.2 x 10^ -7
Explanation: move the decimal until there is one number in front of the decimal and then count how many places you moved the decimal and because it becomes a smaller number, the exponent is negative
