Albinism, lack of pigmentation in humans, is an autosomal recessive disorder. a normally pigmented woman who has an albino uncle wishes to marry a phenotypically normal man whose sister is an albino. (assume that these are the only individuals known to be albino in the two families) what is the probability that the couple's first child is an albino? unless there is evidence to the contrary, all individuals marrying into the family are assumed to be homozygous.

g1

choices:

a. g2. b. g1. c. m

cell division has two checkpoints namely, g1

checkpoint and spindle assembly checkpoint. the checkpoint which determines if

division has properly occurred is the g1 checkpoint. at this point, is a damage

in the dna is detected or  the has not reach the optimum size, the cell is

stopped in g1 and is not allowed to proceed to further process.

source:

substitution is the answer in this case

i think that you are smart and you should fit for it out

i believe it is c: genes for body color and wing size are inherited separately from each parent.