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 17GP
Imagine that a newly discovered, recessively inherited disease is expressed only in individuals with type O blood, although the disease and blood group are independently inherited. A normal man with type A blood and a normal woman with type B blood have already had one child with the disease. The woman is now pregnant for a second time. What is the probability that the second child will also have the disease?
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Duchenne muscular dystrophy is sex linked and usually affects only males. Victims of the disease become progressively weaker, starting early in life.a. What is the probability that a woman whose brother has Duchenne’s disease will have an affected child?b. If your mother’s brother (your uncle) had Duchenne’s disease, what is the probability that you have received the allele?c. If your father’s brother had the disease, what is the probability that you have received the allele?
Duchenne muscular dystrophy is sex linked and usuallyaffects only males. Victims of the disease become progressively weaker, starting early in life.a. What is the probability that a woman whose brotherhas Duchenne’s disease will have an affected child?b. If your mother’s brother (your uncle) had Duchenne’sdisease, what is the probability that you have receivedthe allele?c. If your father’s brother had the disease, what is theprobability that you have received the allele?
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
- Sickle cell anemia is inherited as an autosomal recessive condition. It also exhibits incomplete dominance in that the heterozygous genotype displays a mild form of the disease known as sickle cell trait while individuals with the homozygous recessive genotype have a severe form of SCA. A man who has severe sickle cell anemia marries a woman who suffers from a mild trait. What is the probabilitu they will have a child with severe SCA?What is the probability they will have a child with mild SCA? What is the probability they will have a normal child? Show ALL work using punnett squares.arrow_forwardIn man, muscular dystrophy is a condition in which the muscles waste away during early life and may result in a shorter life expectancy. It is due to a sex-linked, recessive gene. A certain couple has five children – three boys (ages 1yr, 3yrs, and 10yrs old) and two girls (ages 5yrs and 7yrs old). The oldest boy shows the symptoms of this disease. You are their family physician and they come to you for advice. What would you tell them about the chances of their other children developing the disease?arrow_forwardHemophilia is an X-linked recessive phenotype. Suppose a man who expresses the hemophilia phenotype has children with a woman who has the normal phenotype (and does not have a family history of hemophilia). If the couple have a son, what are the chances that he will have hemophilia? A) 50% B) 25% C) 0% D) 100%arrow_forward
- One 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_forwardIn humans, the ABO blood type is under the control of autosomal multiple alleles. Color blindness is a recessive X-linked trait. If two parents who are both type A and have normal vision produce a son who is color blind and is type O, what is the probability that their next child will be a female who has normal vision and is type O?arrow_forwardIn humans, the ABO blood type is under the control of autosomal multiple alleles. Color blindness is a recessive X-linked trait. If two parents who are both type A and have normal vision produce a son who is color-blind and is type O, what is the probability that their next child will be a female who has normal vision and is type O?arrow_forward
- Hemophilia is another example of an X-linked disease caused when a recessive allele (Xh) is expressed. If a normal male reproduces with a heterozygous normal female, what are the expected genotypes and phenotypes? Will any of their daughters develop hemophilia?arrow_forwardPorphyria is a genetic disorder caused by the inability to properly metabolize a component of hemoglobin. King George III is suspected to have been afflicted with this disorder. Assume that both George and his Queen suffered from this disorder and they had one afflicted child and one normal child. Is porphyria inherited in a dominant or recessive fashion? What must be the genotype of both George and his Queen? Using punnett square, show ALL work used to achieve your answer.arrow_forwardAchondroplasia is a form of dwarfism in humans. It is caused by a mutant allele of the fibroblast growth factor receptor 3 gene ( FGFR3) that produces an overactive protein. Having one copy of the mutant allele results in dwarfism. Two copies of the mutant allele results in death before birth. If a man with Achondroplasia marries a woman who is Sickle Cell Anemia carrier and they have a child together, what is the probability that their child will Achondroplasia AND be a Sickle Cell Anemia carrier? ½ 2/3 ¼ 1 ½ 1/16arrow_forward
- Hemophilia A is caused by a recessive X-linked allele that encodes a defective form of a clotting protein. If a affected father and a mother who is known to not be a carrier have children, what percentage of female offspring will have hemophilia?arrow_forwardThe following pedigree shows the inheritance of Huntington’s disease, a fatal genetic disorder that causes neurodegeneration. Since signs and symptoms usually do not appear until adulthood, many who are carriers may not realize their risk of passing on the disease-causing allele. The following pedigree represents a family in which some people are affected by Huntington’s disease. Using just the information on this pedigree, is Huntington’s disease caused by a dominant allele or recessive alleles? What are the genotypes of the grandparents (I-1 and I-2)? What are the genotypes of the parents (II-6 and II-7)? If the parents above have another child, what is the chance that they will be affected by the Hungtington’s disease allele? What are the genotypes of the unaffected children (III-8, 9, 10)? What is the chance that the unaffected children above will pass on a Huntington’s disease allele to their children? What is the genotype of the affected child (III-11)? What is the chance…arrow_forwardSuppose a woman who is a carrier of sickle-cell trait (making her a heterozygote) has children with a man who is totally healthy and does not carry the gene for sickle-cell trait at all. Which one of the following is true about their potential children? (Draw a Punnett square on scratch paper if it helps you.) A) None of their children will have sickle-cell disease. B) All of their children will have sickle-cell disease. C) All of the couple's children would be heterozygous carriers like the mother.arrow_forward
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