Answer:
50% for sons 0%for daughters
Explanation:
the genotype of the mother is X⁻X
the genotype of the father is XY
the gametes from the mother are X⁻ andX
the gametes from the father are X and Y
to find the chance we make a Punnet square and cross each gamete
1 of the 2 males has the gene for colorblindness so there is a 50% chance that the son will be colorblind
1 of the 2 daughters has the gene for cloroblindness but only in one exemplary so the chance is 0%
The correct answer of the given question above would be PROTEIN. The macromolecule that is involved in nearly every function in the human body is the protein. I<span>f there is a shortage of carbohydrates or lipids, proteins can serve as an energy source. It is also essential in building muscle mass. Hope this answer helps.</span>
Answer:
Cone dystrophy is manifested by the loss of acute visual acuity (which cannot be corrected with glasses), severe sensitivity to light (photophobia) and blind spots (scotomas) in the peripheral vision, which progress and produce poor vision in dimly lit or dark environments ("night blindness") and total loss of the peripheral visual field, which can be progressive.
Explanation:
Rod and cone dystrophies (CRDs) are inherited retinal dystrophies. They are included in the group of retinitis pigmentosa, and, more generally, in that of retinopathy pigmentosa. Cones are responsible for color and detail vision. Cone dystrophy is a disease of hereditary degeneration of the cone receptors, whose hallmark includes the "trilogy" of progressive loss of central visual acuity, disturbance in color vision and sensitivity to light (photophobia) which can be progressive.
It might be because it is close to the earth
Hope this helps!