Study Guide for Campbell Biology
11th Edition
ISBN: 9780134443775
Author: Lisa A. Urry, Michael L. Cain, Steven A. Wasserman, Peter V. Minorsky, Jane B. Reece, Martha R. Taylor, Michael A. Pollock
Publisher: PEARSON
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Chapter 14, Problem 8IQ
Consider the following pedigree for the trait albinism (lack of skin pigmentation) in three generations of a family. (Solid symbols represent individuals with albinism.) From your knowledge of
- a. Is this trait caused by a dominant or recessive allele? How can you tell?
- b. Determine the genotypes of the parents in the first generation. (Let A and a represent the alleles.) Genotype of father _____; genotype of mother _____. How can you tell?
- c. Determine the probable genotypes of the mates of the offspring with albinism in the second generation and grandson #4 in the third generation. Genotypes: mate #1 _____; mate #2 _____; grandson #4 _____.
- d. Can you determine the genotype of son #3 in the second generation? Why or why not?
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Phenylketonuria (PKU) is a disorder caused by a recessive allele. Two carrier individuals have progeny. Answer the following questions in order and show solutions whenever relevant.
a. Indicate the gene notation.b. Derive the expected genotypic and phenotypic ratios.c. If they have a normal child, what is the probability that he or she will be heterozygous?d. If they have three children, what is the probability of having 2 affected children and one normalchild?
Please consider the following pedigree. Assume that people who marry in to the family do not carry the allele unless otherwise indicated. Assume complete penetrance.
image attached
a. Is it possible for the inheritance pattern for the trait illustrated in this pedigree to be as a result of each of the following? Answer yes or no. (i) an autosomal recessive allele (AR)(ii) an autosomal dominant allele (AD)(iii) a X-linked recessive allele (XR)(iv) a X-linked dominant allele (XD) b. Provide a set of parents that definitively supports your answers in (a).
Huntington diseases is a rare fatal, degenerative neurological disease in which individuals start to show symptoms in their 40s. It is caused by a dominant allele. Joe, a man in his 20s, just learned that his father has Huntington disease.a. What is the probability that Joe will also develop the disease?b. Joe and his new wife have been eager to start a family. What is the probability that their first child will eventually develop the disease?
Chapter 14 Solutions
Study Guide for Campbell Biology
Ch. 14 - Fill in the following diagram of a cross of...Ch. 14 - A tall pea plant is crossed with a recessive dwarf...Ch. 14 - A true-breeding tall, purple-flowered pea plant...Ch. 14 - a. In the following cross, what is the probability...Ch. 14 - Prob. 5IQCh. 14 - Consider an example in which the M/m gene (for...Ch. 14 - The height of spike weed is a result of polygenic...Ch. 14 - Consider the following pedigree for the trait...Ch. 14 - a. What is the probability that a mating between...Ch. 14 - If two prospective parents both have siblings who...
Ch. 14 - Prob. 1SYKCh. 14 - How many different types of gametes can be formed...Ch. 14 - Prob. 3SYKCh. 14 - _______ gene Description a. has no effect on...Ch. 14 - _________ allele Description a. has no effect on...Ch. 14 - Prob. 3TYKMCh. 14 - Prob. 4TYKMCh. 14 - __________ dominant allele Description a. has no...Ch. 14 - __________ recessive allele Description a. has no...Ch. 14 - __________ genotype Description a. has no effect...Ch. 14 - Prob. 8TYKMCh. 14 - Prob. 9TYKMCh. 14 - Prob. 10TYKMCh. 14 - Prob. 11TYKMCh. 14 - Prob. 12TYKMCh. 14 - According to Mendels law of segregation, a. there...Ch. 14 - The F2 generation a. has a phenotypic ratio of...Ch. 14 - A 1:1 phenotypic ratio in a testcross indicates...Ch. 14 - Which phase of meiosis is most directly related to...Ch. 14 - After obtaining two heads from two tosses of a...Ch. 14 - The probability of tossing three coins...Ch. 14 - The probability of tossing three coins...Ch. 14 - In the F2 of a dihybrid cross involving two...Ch. 14 - In guinea pigs, the brown coat color allele (B) is...Ch. 14 - A true-breeding dwarf corn plant with red ears is...Ch. 14 - Prob. 11TYKCh. 14 - Prob. 12TYKCh. 14 - Prob. 13TYKCh. 14 - In humans, earwax can be wet or dry. The form of...Ch. 14 - You have blood type B, your mother has blood type...Ch. 14 - Prob. 16TYKCh. 14 - Summer squash are either white or yellow. To get...Ch. 14 - Prob. 2GPCh. 14 - True-breeding tall red-flowered plants are crossed...Ch. 14 - Prob. 4GPCh. 14 - Prob. 5GPCh. 14 - Prob. 6GPCh. 14 - Prob. 7GPCh. 14 - Prob. 8GPCh. 14 - Prob. 9GPCh. 14 - Fur color in rabbits is determined by a single...Ch. 14 - Prob. 11GPCh. 14 - The ability to taste phenylthiocarbamide (PTC) is...Ch. 14 - Prob. 13GPCh. 14 - Prob. 14GPCh. 14 - Prob. 15GPCh. 14 - Prob. 16GPCh. 14 - Imagine that a newly discovered, recessively...Ch. 14 - In mice, black fur (B) is dominant to white (b)....
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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
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- Several members of the family in the pedigree who suffered from a disease are colored in black. Currently deceased members of the family are struck out with a line. a. Based on the data in the pedigree, propose a Mendelian model that would explain the inheritance of this disease. Explain how the data is consistent with your model. b. A scientist hypothesizes that a mutation at a single locus is responsible for the pattern of inheritance seen in this pedigree. Explain how a mutation in a gene can arise during meiosis. Describe one strategy organisms use to prevent such mutations from arising. I II Ø- III TI IV of 22 Answered 딤 F3 F5 @ %23 $4 % 2 3 5 8 W Y S F Garrow_forwardTay-Sachs disease is a rare human disease in which toxic substances accumulate in nerve cells. The recessive allele responsible for the disease is inherited in a simple Mendelian manner. For unknown reasons, the allele is more common in populations of Ashkenazi Jews of eastern Europe. A woman is planning to marry her first cousin, but the couple discovers that their shared grandfather’s sister died in infancy of Tay-Sachs disease.a. Draw the relevant parts of the pedigree, and show all the genotypes as completely as possible. b. What is the probability that the cousins’ first child will have Tay-Sachs disease, assuming that all people who marry into the family are homozygous normal?arrow_forwardThe condition phenylketonuria is caused by a recessive allele. There are two carriers who have progeny.a. Give the gene notation. b. Give the expected genotypic and phenotypic ratios. c. What is the probability that their child will be heterozygous if they have a normal child?d. What is the probability of having two affected children and one normal child if they have three children?arrow_forward
- Look at the pedigree below and answer the following questions related to the human genetic trait depicted in this pedigree. 1. Indicate whether the pattern of inheritance associated with this human trait is most likely to be (i) rare X-linked recessive, (ii) sex-influenced, or (iii) sex-limited. You may assume that the gene is fully penetrant. Then, provide a specific reason that justifies your selection of this pattern of inheritance as the correct one, and also explain why each of the other two alternatives are not correct. As part of your answer, include the phenotypic ratio, including the sex of the offspring, that you would expect to find in each of the three possible scenarios.arrow_forwardPedigree analysis is often used to determine mode of inheritance (dominant or recessive, for example). Be sure to read the "Tips for Pedigree Analysis" in Figure 14.15 in 34. your text. Consider the following pedigree for the trait albinism (lack of skin pigmentation) in three generations of a family. (Solid symbols represent individuals with albinism.) Complete the unlabeled pedigree by indicating the genotypes for all involved. From your knowledge of Mendelian inheritance, answer the questions that follow. a. Is this trait caused by a dominant or recessive allele? What is the evidence for your response?arrow_forwardRed-green color blindness is inherited as an X-linked recessive (Xc). If a color-blind man marries a woman who is heterozygous for normal vision, what would be the expected phenotypes of their children with reference to this character? In your answer, specify in your phenotype descriptions the gender of the children. (For example, don’t just say 75% of the children would be colorblind – you would instead say 100 % of the daughters would be colorblind and 50% of the sons would be colorblind. Note that this is not a correct answer; it is just to give you an idea of how to explain the correct phenotypes of the cross.)___arrow_forward
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