EBK CAMPBELL BIOLOGY IN FOCUS
2nd Edition
ISBN: 8220101459299
Author: Reece
Publisher: PEARSON
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Chapter 11, Problem 9TYU
Summary Introduction
To determine:
The probability of the offspring of Karen and Steveto have sickle cell anemia, if both of them have siblings who had sickle cell anemia.
Introduction:
Sickle cell anemia is a disease in which the red blood corpuscles are sickle shaped or crescent shapedrather than round with a grove in the middle. This is caused due to a mutation in one of the base pairs and it is a hereditary disease. It causes the loss in binding of oxygen molecule to red blood cells.
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Chapter 11 Solutions
EBK CAMPBELL BIOLOGY IN FOCUS
Ch. 11.1 - DRAW IT Pea plants heterozygous for flower...Ch. 11.1 - List all gametes that could be made by a pea plant...Ch. 11.1 - Prob. 3CCCh. 11.2 - For any gene with a dominant allele A and...Ch. 11.2 - Two organisms, with genotypes BbDD and BBDd, are...Ch. 11.2 - Prob. 3CCCh. 11.3 - Incomplete dominance and epistasis are both terms...Ch. 11.3 - Prob. 2CCCh. 11.3 - WHAT IF? A rooster with gray feathers and a hen of...Ch. 11.4 - Beth and Tom each have a sibling with cystic...
Ch. 11.4 - MAKE CONNECTIONS In Table 11.1, note the...Ch. 11 - DRAW IT Two pea plants heterozygous for the...Ch. 11 - A man with type A blood marries a woman with type...Ch. 11 - A man has six fingers on each hand and six toes on...Ch. 11 - Prob. 4TYUCh. 11 - Flower position, stem length, and seed shape are...Ch. 11 - Prob. 6TYUCh. 11 - Prob. 7TYUCh. 11 - Prob. 8TYUCh. 11 - Prob. 9TYUCh. 11 - Prob. 10TYUCh. 11 - In tigers, a recessive allele that is pleiotropic...Ch. 11 - Prob. 12TYUCh. 11 - Imagine that you are a genetic counselor, and a...Ch. 11 - Prob. 15TYUCh. 11 - Prob. 16TYUCh. 11 - Prob. 17TYU
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- Cystic fibrosis (CF) is an autosomal recessive trait (a). Assume that Emily (who has CF) decides to have children with a man who does not have CF and who is not a carrier of CF. What are their genotypes, and what is the probability that they will have a child who is a carrier for CF?arrow_forwardMark has an autosomal recessive condition called sickle cell anemia, a serious blood disorder that is associated with painful complications. His spouse has not experienced symptoms of sickle cell anemia but their first child developed the disease. What conclusions can be drawn about the mother's genotype and the probability of having a second child with the condition? Answer Choices: A: her genotype is heterozygous and there is a 25% percent chance of having another child with the disorder B: her genotype is heterozygous and there is a 50% percent chance of having another child with the disorder C: her genotype is heterozygous and there is a 75% percent chance of having another child with the disorder D: she lacks the allele for sickle cell anemia in that she lacks symptoms of the disease. There is a 0% percent chance of having another child with the disorderMark has an autosomal recessive condition called sickle cell anemia, a serious blood disorder that is associated with…arrow_forwardMarly is doing a paternity test to determine who could be her father. She is going just off of word of mouth for now so there is no way for her to figure out the genotypes of ther potential fathers. She knows for certain that she is type A with the genotype (A^I A^i). Her potential fathers are Gayle who is a Type O, Jake who is type A,and Mark who is Type AB. Who could be the potential father?arrow_forward
- Because Elsa has received a confirmed diagnosis of beta-thalassemia major, which of the following statements is true about her parents? Only her mother carried the gene that caused her blood disorder. Only her father carried the gene that caused her blood disorder. If her parents have another child naturally, there is a 100% chance that the second child will be diagnosed with beta-thalassemia major. If her parents have another child naturally, there is a 25% chance that the second child will be diagnosed with beta-thalassemia major.arrow_forwardHemophilia 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_forwardKaren and Steve each have a sibling with sickle-cell disease.Neither Karen nor Steve nor any of their parents have thedisease, and none of them have been tested to see if they carrythe sickle-cell allele. Based on this incomplete information,calculate the probability that if this couple has a child, thechild will have sickle-cell disease.arrow_forward
- Hemophilia is due to a sex-linked gene. It is recessive and found on the X chromosome. A woman who is a carrier for hemophilia marries a normal man. What will be the possible phenotypes of their children? (use the letter “H”)arrow_forwardA certain couple has six children – four boys (ages 2yr, 5yrs, 9yrs and 11yrs old) and two girls (ages 5yrs and 7yrs old). The oldest boy shows the symptoms of Duchenne Muscular Dystrophy (DMD). What are the chances of their other children developing the disease?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
- The following is a summary of the possible sickle-cell genotypes and phenotypes: AA - cojmpletely normal AS - sickle-cell trait (this person has a combination of normal hemoglobin and the abnormal, sickled form of hemoglobin) SS - sickle-cell anemia (all abnormal hemoglobin) Make a punnett square for help answering the question: What is the probability of a couple having a child with sickle-cell trait if one parent is normal and the other has sickle-cell trait?arrow_forwardBoth parents love strawberry blonde hair but hate the fact they can touch their noses with their tongues. What are the odds their child will be a strawberry blonde non-nose touching individual?arrow_forwardMary has type O blood type . Frank has homozygous type B blood type. Mary had a child with type O blood type. Can frank be the father of this child? Why or why not?arrow_forward
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