If a woman heterozygous for colorblindness has a child by a man who is colorblind.
What percentage of the daughters will be colorblind?

Monitor and apply fix up strategies

Tay-sachs disease is caused by a mutation in the hexa gene located on chromosome 15. tay-sachs follows an autosomal recessive pattern of inheritance. with the of the diagram, identify which of the offspring will be an unaffected carrier. a diagram showing the genes of parents who are carriers of tay-sachs disease a. a, b, and c b. b and c c. a and d d. a e. d

Which of these definitions have been paired with the correct type of cell?