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?
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?
Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:Elaine N. Marieb, Katja N. Hoehn
Chapter1: The Human Body: An Orientation
Section: Chapter Questions
Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...
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![Explain your answer. Below is a pedigree showing the inheritance of colorblindness in
Akoto family. Çolorblindness is a recessive and X-linked trait (X-). The allele for normal
vision is dominant and is represented by Xe.
2
II
IV
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?](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F01afc5bf-e4b3-4f9a-b6d8-5f21a570aedf%2Fbfa81f69-4b95-4643-969f-5dfa17b8e71b%2F7wdvyot_processed.jpeg&w=3840&q=75)
Transcribed Image Text:Explain your answer. Below is a pedigree showing the inheritance of colorblindness in
Akoto family. Çolorblindness is a recessive and X-linked trait (X-). The allele for normal
vision is dominant and is represented by Xe.
2
II
IV
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?
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