EBK BIOLOGY
5th Edition
ISBN: 9780133996807
Author: Maier
Publisher: PEARSON CUSTOM PUB.(CONSIGNMENT)
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Chapter 7, Problem 4GP
Summary Introduction
To determine:
The genotype of the parents, if they are normal and produce an albino child.
Introduction:
The allele is the form of a single gene present in an organism. The different combination of the alleles determines the genotype and
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Albinism is a recessive trait. Two individuals who both have normal pigmentation have one child out of three who has albinism (without melanin pigmentation). What are the genotypes of this child's parents?
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Mary is concerned that she may be a carrier for
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In humans, having freckles is dominant to not having freckles. What is the genotype of a person without freckles?
Chapter 7 Solutions
EBK BIOLOGY
Ch. 7 - What is the relationship between genotype and...Ch. 7 - Prob. 2LTBCh. 7 - Prob. 3LTBCh. 7 - Prob. 4LTBCh. 7 - Prob. 5LTBCh. 7 - Scientists have recently developed a process by...Ch. 7 - What is the physical basis for the independent...Ch. 7 - Prob. 8LTBCh. 7 - Prob. 9LTBCh. 7 - Prob. 10LTB
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Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.Similar questions
- Hemophilia is a sex-linked recessive trait. A male hemophiliac and phenotypically normal female have a son with hemophilia. They would like to have one more child. What is the probability of having a child without hemophilia? Explain using a Punnett square. Is it possible for a girl to be born with hemophilia? Explain.arrow_forwardAlbinism is inherited through a recessive allele (a). Juan has normal skin color. His Mom and Dad also have normal skin color. Juan marries Paige, who also has normal skin color. Surprisingly, their first child is an albino. What is everyone's genotype?arrow_forwardOne form of the bleeding disorder known as von Willebrand disease is an autosomal recessive disease. A man who is a carrier marries a woman who is also a carrier of the disease. (a) What percentage of their children are likely to have a disease phenotype? (b) What percentage of their children are likely to have a normal phenotype? (c) What percentage of their children are likely to be carriers of the disease?arrow_forward
- A woman homozygous dominant for albinism marries a man who is homozygous recessive for albinism. What are the possible genotypes and phenotypes for their offspring? What are the ratios?arrow_forwardA woman homozygous dominant for albinism marries a man who is homozygous recessive for albinism. What are the possible genotypes and phenotypes percentages for their offspring?arrow_forwardAlbinism causes the skin, hair, or eyes to have little or no color. It is also associated with vision problems. Albinism results from an allele a that is recessive to the allele for normal melanin production. Maya has normal skin color, but her sister has albinism. Maya’s mother has albinism, and her father has normal skin color. a)What are the genotypes of Maya, her sister, her mother, and her father. b)If Maya’s parents have another child, what is the probability that this child will have albinism? Show the Punnett square you use to help in solving. c)If Maya marries a man with albinism, what is the probability that their first child will have albinism? Show the Punnett square you use to help in solving.arrow_forward
- Johnny has unattached earlobes (a dominant trait) like his father, but his mother has attached earlobes. What is johnny’s genotype?arrow_forwardJim and the members of his family do not have freckles. His maternal grandfather has freckles. What is the genotype of his maternal grandfather?arrow_forwardIn humans, normal skin color (A) is dominant over albino (a). An albino man marries a normal woman whose mother was an albino and whose father has normal skin color. What is the genotype of the man and the woman? What proportion of their children would be expected to be both normal skin pigmentation and have the trait for albino?arrow_forward
- For a recessive condition, two normal heterozygous individuals have children. What is the likelihood of their children being affected by this condition? What is the likelihood of their children being carriers without the condition? What is the likelihood of their asymptomatic children being carriers? Suppose that an individual with the condition has children with a heterozygous individual, what is the likelihood of their children being carriers?arrow_forwardAlbinism is a recessive disorder where there is a lack of melanin. Andrea and her husband Claude both have normal skin pigmentation. Andrea’s mother has the albino phenotype, but her father and her brother do not (normal pigmentation). Claude’s parents are both normal, but he has a sister who has the condition (is albino). Answer the following questions If Andrea and Claude are carriers for the albino allele, what is the probability that they have an albino child? If Andrea and Claude have a second child, what is the probability this child be normal (non-albino)? NOTE: Draw a punnet square or show your work.arrow_forwardSkin color in humans is determined by a polygenic inheritance system. The husband is white while the wife is of Nigerian heritage. However, their two children are all light-skinned. How were the married couples able to have light-skinned babies. Are the odds to have a light-skinned baby one in a million? What are the possible genotypes of the husband and the wife and their children.arrow_forward
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