Final answer:
Frank's genotype is XoY since he's colorblind, and Awilda's genotype is XX because she has no family history of color blindness. Sons of Frank and Awilda have a 50% chance of being colorblind while it's impossible for their daughters to be colorblind, but they may be carriers.
Step-by-step explanation:
The genotypes of Frank and Awilda can be determined based on the inheritance patterns of color blindness, which is an X-linked recessive trait. Since Frank is colorblind and male, his genotype must be XoY. Awilda, not being colorblind and having no family history of colorblindness, is likely to have a normal genotype of XX. If Awilda had a colorblindness gene, she would be a carrier with genotype XoX, but it is suggested that she doesn't carry the trait at all due to her family history. Therefore, it is incorrect to assert that males can be carriers of red-green color blindness, as it is X-linked recessive, not autosomal dominant.
To have a daughter who is colorblind, both parents must contribute an X chromosome with the recessive colorblind gene. In Frank and Awilda's case, since Frank has an affected X chromosome but Awilda has two normal X chromosomes, their sons have a 50% chance of being colorblind (inheriting Frank's Xo), while their daughters cannot be colorblind—they can only be carriers if they inherit Frank's Xo chromosome.