Campbell Essential Biology with Physiology (6th Edition)
6th Edition
ISBN: 9780134711751
Author: Eric J. Simon, Jean L. Dickey, Jane B. Reece
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 9, Problem 3SQ
Summary Introduction
Introduction: Edward was found to be heterozygous (Ss) for the sickle-cell trait. In this disease the effect of a single gene on a chromosome is amplified. It affects many genes coding for sickle cell anemia. The shape of the red blood cells changes and they become crescent shaped. They ability to bind to oxygen decreases in blood. The dominant gene for sickle cell anemia in the genotype is represented by S and the recessive gene in the genotype is represented by s. The depiction for hemoglobin is depicted by Hb and in a cross it can be depicted as
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
Hemophilia is a disease caused by a gene found on the X
chromosome. Therefore, it is referred to as a sex-linked disease.
The recessive allele causes the disease. A man with hemophilia
(xhy) marries a woman who is homozygous dominant (XHXH.
A. Illustrate using a Punnett square the probability that their children
will have the disease.
B. Will any of their children have the disease?
C. Predict the probabilities of their children having the disease.
Hemophilia is a disease caused by a gene found on the X chromosome. Therefore, it is a sex-linked disease which is caused by the recessive allele. Suppose, a man with hemophilia marries a woman who is homozygous dominant for the trait, what is the chance of having children who are hemophiliacs? (XH = normal; Xh= hemophiliac) *
a. 0%
b. 75%
c. 100%
d. 25%
Edward was found to be heterozygous (Ss) for the sickle-cell trait. The alleles represented by the letters S and s are a. on the X and Y chromosomes. b. linked. c. on homologous chromosomes. d. both present in each of Edward’s sperm cells.
Chapter 9 Solutions
Campbell Essential Biology with Physiology (6th Edition)
Ch. 9 - The genetic makeup of an organism is called its...Ch. 9 - Which of Mendels laws is represented by each...Ch. 9 - Prob. 3SQCh. 9 - Prob. 4SQCh. 9 - Prob. 5SQCh. 9 - Prob. 6SQCh. 9 - Prob. 7SQCh. 9 - Prob. 8SQCh. 9 - Prob. 9SQCh. 9 - Prob. 10SQ
Ch. 9 - Prob. 11SQCh. 9 - Prob. 12SQCh. 9 - Incomplete dominance is seen in the inheritance of...Ch. 9 - Why was Henry VIII wrong to blame his wives for...Ch. 9 - Prob. 15SQCh. 9 - Prob. 16SQCh. 9 - Prob. 17SQCh. 9 - Prob. 18IMTCh. 9 - Prob. 19IMTCh. 9 - Prob. 20IMTCh. 9 - Prob. 21PSCh. 9 - Prob. 22PSCh. 9 - Prob. 23BSCh. 9 - Gregor Mendel never saw a gene, yet he concluded...Ch. 9 - Prob. 25BS
Knowledge Booster
Learn more about
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
- A man who has color blindness and type O blood has children with a woman who has normal color vision and type AB blood. The woman’s father had color blindness. Color blindness is determined by an X-linked gene, and blood type is determined by an autosomal gene. a. What are the genotypes of the man and the woman? b. What proportion of their children will have color blindness and type B blood? c. What proportion of their children will have color blindness and type A blood? d. What proportion of their children will be color blind and have type AB blood?arrow_forwardDuchenne 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?arrow_forwardWhat is the phenotype of a person who has XXXY sex chromosomes? a. Klinefelter syndromeb. Turner syndromec. Poly-X femalearrow_forward
- In humans, hemophilia is an X-linked recessive condition characterized by the inability of blood to clot normally. A woman who is a carrier for hemophilia marries a man who has hemophilia. What are the genotypes of the woman and man, respectively? a. xH+xH+, xH+y b. xH+xH xH+y c. xH+xH xHy Od. XHXH, XH+y O e. xHxH xHyarrow_forwardChoose the statement that is incorrect.a. A son can inherit a recessive allele on anX chromosome from either parent.b. An individual may inherit three or more of eachtype of chromosome characteristic of the species, acondition called polyploidy.c. A female child inherits one X chromosome from hermother and one from her father.d. Pedigree analysis can be used to determine a futurechild’s chance of being born with achondroplasiaarrow_forwardEarlobes can be attached to the face or non-attached. An attached earlobe is a recessive trait. A female with attached earlobes (Il) has a child with a man with non-attached earlobes. He is heterozygous for this trait. Questions: a. What are the possible genotypes of the egg the woman can produce? b. What are the possible genotypes of the sperm the man can produce? c. What is the genotype ratio for the offspring? d. What is the phenotype ratio for the offspring? e. What is the couple's chance of having a child with attached earlobes?arrow_forward
- Red–green color blindness is a human X-linked recessive disorder. Jill has normal color vision, but her father is color blind. Jill marries Tom, who also has normal color vision. Jill and Tom have a daughter who has Turner syndrome and is color blind. a. How did the daughter inherit color blindness? b. Did the daughter inherit her X chromosome from Jill or from Tom?arrow_forwardHemophilia is a disease caused by a recessive allele (h), which is found on the X chromosome, non-hemophilia is (H). A normal man marries a woman that is heterozygous for the trait. Give the genotypes and phenotypes of all possible offspring?arrow_forwardHemophilia is called "the royal disease" because many European royal families had members with the condition. Hemophilia is a recessive, X-linked disorder. Queen Victoria was unaffected by hemophilia, but was a carrier of the hemophilia gene (X X ). Suppose Queen Victoria's husband, Prince Albert, was affected with hemophilia (X Y). What is the percent probability that a son of Queen Victoria and Prince Albert would be unaffected by hemophilia? probability of unaffected son: What is the percent probability that a daughter or son of Queen Victoria and Prince Albert would be affected by hemophilia? probability of affected child: What is the percent probability Queen Victoria and Prince Albert would have two affected females? probability of two affected females: % % %arrow_forward
- A woman with a rare autosomal recessive disorder was told that it was unlikely that her children would have the disorderas her husband did not have it. However, her first child has the disorder. a. What is the most likely explanation? b. Diagram the cross between the woman and her husband using a Punnett square, give the genotypic ratio (GR) and phenotypic ratio (PR) from the Punnett square. c. Based on the Punnett square results, what is the chance that her next child will have the disorder?arrow_forwardChoose correct option and do explain. Considering an X-linked dominant trait, if an affected woman and an unaffected man decide to have children, which of the answer choices is possible for their children? a. All of their sons are expected to show the dominant trait. b. Their daughters are expected be heterozygous for the gene. c. Their daughters are not expected to show the dominant trait. d. Their sons are expected to be heterozygous for the gene. e. All their children, whether male or female, are expected to show the dominant trait.arrow_forwardAssume that one of Merida's sons, who is heterozygous for orange hair color, married a girl that was also heterozygous. Create a Punnett square to show the possibilities that would result if they had children. a. List the possible genotypes and phenotypes for their children. b. What are the chances of a child with orange hair? c. What are the chantes of a child with yellow?arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Concepts of BiologyBiologyISBN:9781938168116Author:Samantha Fowler, Rebecca Roush, James WisePublisher:OpenStax College
Concepts of Biology
Biology
ISBN:9781938168116
Author:Samantha Fowler, Rebecca Roush, James Wise
Publisher:OpenStax College
How to solve genetics probability problems; Author: Shomu's Biology;https://www.youtube.com/watch?v=R0yjfb1ooUs;License: Standard YouTube License, CC-BY
Beyond Mendelian Genetics: Complex Patterns of Inheritance; Author: Professor Dave Explains;https://www.youtube.com/watch?v=-EmvmBuK-B8;License: Standard YouTube License, CC-BY