Explain your answer. Below is a pedigree showing the inheritance of colorblindness in Akoto family. Colorblindness is a recessive and X-linked trait (X-). The allele for normal vision is dominant and is represented by X•. 모오 1 2 2 IV 2 1. What are the genotypes of the founding parents (I-1, I-2)? 2. What is the percentage of the affected offspring (II)? 3. What is the phenotype of III-2? 4. Is the inheritance autosomal or sex-linked?

Please help finding the chance. Correct answer is 1/32

Directions: Use the following information to answer the questions below: all are sex-linked recessive disorders. H= normal blood clotting C=Normal Vision h-hemophilia muscular dystrophy M= Normal c= colorblind 1. Write the genotypes for the following individuals: a. female with no family history of hemophilia b. male with hemophilia c. male with muscular dystrophy d. male with normal color vision e. normal color vision female with colorblind father f. male with normal blood clotting g. colorblind male m= 2. Cross a female who is a carrier of the gene for hemophilia with a man who has normal blood clotting. Tell the expected phenotypic ratio of the offspring. 3. Cross a female with normal color vision, but whose father was colorblind, with a man who has colorblindness. Tell the expected phenotypic ratio of the offspring. 4. Cross a woman who does not suffer from muscular dystrophy and has no family history of muscular dystrophy with a man who has the disorder. Tell the expected…

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