Genetics: From Genes to Genomes
6th Edition
ISBN: 9781259700903
Author: Leland Hartwell Dr., Michael L. Goldberg Professor Dr., Janice Fischer, Leroy Hood Dr.
Publisher: McGraw-Hill Education
expand_more
expand_more
format_list_bulleted
Concept explainers
Textbook Question
Chapter 2, Problem 10P
In humans, a dimple in the chin is a dominant characteristic controlled by a single gene.
a. | A man who does not have a chin dimple has children with a woman with a chin dimple whose mother lacked the dimple. What proportion of their children would be expected to have a chin dimple? |
b. | A man with a chin dimple and a woman who lacks the dimple produce a child who lacks a dimple. What is the man’s genotype? |
c. | A man with a chin dimple and a non-dimpled woman produce eight children, all having the chin dimple. Can you be certain of the man’s genotype? Why or why not? What genotype is more likely, and why? |
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
In humans, a dimple in the chin is a dominant characteristic controlled by a single gene.a. A man who does not have a chin dimple haschildren with a woman with a chin dimple whose mother lacked the dimple. What proportion of theirchildren would be expected to have a chin dimple?b. A man with a chin dimple and a woman who lacksthe dimple produce a child who lacks a dimple.What is the man’s genotype?c. A man with a chin dimple and a nondimpledwoman produce eight children, all having the chindimple. Can you be certain of the man’s genotype?Why or why not? What genotype is more likely,and why?
In humans, a dimple in the chin is a dominant characteristic controlled by a single gene.
A man who does not have a chin dimple has children with a woman with a chin dimple whose mother lacked the dimple. What proportion of their children would be expected to have a chin dimple?
A man with a chin dimple and a woman who lacks the dimple produce a child who lacks a dimple. What is the man’s genotype?
A man with a chin dimple and a non-dimpled woman produce eight children, all having the chin dimple. Can you be certain of the man’s genotype? Why or why not? What genotype is more likely, and why?
a. Why males and females do not show equal chances of inheriting a trait?
b. Is it possible to determine the genotypes of the parents based on the phenotypes of the offspring?
Chapter 2 Solutions
Genetics: From Genes to Genomes
Ch. 2 - For each of the terms in the left column, choose...Ch. 2 - During the millennia in which selective breeding...Ch. 2 - Describe the characteristics of the garden pea...Ch. 2 - An albino corn snake is crossed with a...Ch. 2 - Two short-haired cats mate and produce six...Ch. 2 - Piebald spotting is a condition found in humans in...Ch. 2 - As a Drosophila research geneticist, you keep...Ch. 2 - A mutant cucumber plant has flowers that fail to...Ch. 2 - In a particular population of mice, certain...Ch. 2 - In humans, a dimple in the chin is a dominant...
Ch. 2 - Some inbred strains of the weedy plant Arabidopsis...Ch. 2 - Among Native Americans, two types of earwax...Ch. 2 - Imagine you have just purchased a black stallion...Ch. 2 - If you roll a die singular of dice, what is the...Ch. 2 - In a standard deck of playing cards, four suits...Ch. 2 - How many genetically different eggs could be...Ch. 2 - What is the probability of producing a child that...Ch. 2 - A mouse sperm of genotype a B C D E fertilizes an...Ch. 2 - Your friend is pregnant with triplets. She thinks...Ch. 2 - Galactosemia is a recessive human disease that is...Ch. 2 - Albinism is a condition in which pigmentation is...Ch. 2 - A cross between two pea plants, both of which grew...Ch. 2 - A third-grader decided to breed guinea pigs for...Ch. 2 - The self-fertilization of an pea plant produced...Ch. 2 - The achoo syndrome sneezing in response to bright...Ch. 2 - A pea plant from a pure-breeding strain that is...Ch. 2 - The following table shows the results of different...Ch. 2 - A pea plant heterozygous for plant height, pod...Ch. 2 - In the fruit fly Drosophila melanogaster, the...Ch. 2 - Based on the information you discovered in the...Ch. 2 - Considering the yellow and green pea color...Ch. 2 - What would have been the outcome the genotypic and...Ch. 2 - Recall that Mendel obtained pure-breeding with...Ch. 2 - The gene that likely controlled flower color...Ch. 2 - For each of the following human pedigrees,...Ch. 2 - Consider the pedigree that follows for cutis laxa,...Ch. 2 - A young couple went to see a genetic counselor...Ch. 2 - Huntington disease is a rare fatal, degenerative...Ch. 2 - Is the disease shown in the following pedigree...Ch. 2 - Figure 2.22 shows the inheritance of Huntington...Ch. 2 - Consider the cystic fibrosis pedigree in Figure...Ch. 2 - Prob. 42PCh. 2 - People with nail-patella syndrome have poorly...Ch. 2 - Midphalangeal hair hair on top of the middle...Ch. 2 - A man with Huntington disease he is heterozygous...Ch. 2 - Explain why disease alleles for cystic fibrosis CF...Ch. 2 - The following pedigree shows the inheritance of...
Additional Science Textbook Solutions
Find more solutions based on key concepts
Describe the evolution of mammals, tracing their synapsid lineage from early amniote ancestors to true mammals....
Loose Leaf For Integrated Principles Of Zoology
1. Genetics affects many aspects of our lives. Identify three ways genetics affects your life or the life of a ...
Genetic Analysis: An Integrated Approach (2nd Edition)
1. The correct sequence of levels forming the structural hierarchy is
A. (a) organ, organ system, cellular, che...
Human Anatomy & Physiology (Marieb, Human Anatomy & Physiology) Standalone Book
How does the removal of hydrogen atoms from nutrient molecules result in a loss of energy from the nutrient mol...
Seeley's Anatomy & Physiology
Why are mutants used as test organisms in the Ames test?
Laboratory Experiments in Microbiology (12th Edition) (What's New in Microbiology)
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. Determine if the pedigree below can be for a trait that is X-linked traits. Write the genotype of each individual next to the symbol. b. Is it possible that this pedigree is for an X-linked recessive trait? c. What can you conclude about the children if both parents are affected with an X-linked recessive trait?arrow_forwardQuestions a to e are answerable by yes or no. Indicate the possible parental genotypes if your answer is yes.a. Can a man with hairy ears have a hairy-eared daughter?b. Can two normal parents produce a colorblind son?c. Can two normal parents produce a colorblind daughter?d. Can a colorblind woman have a normal son?e. Can a bald man have a nonbald daughter?arrow_forwardHair texture is determined by gene c in an incomplete dominance inheritance pattern, where the heterozygous condition (c1c2) results in wavy hair. Hairline is controlled by gene H, where a widow's peak is dominant to a straight hairline. If a woman with curly hair and a straight hairline has a child with a man with a widow's peak and straight hair (his mom had a straight hairline), what is the chance they would have a kid that has exactly the same hair as mom? Draw the Punnett square and demonstrate the possible genotypes and phenotypes that could result from these two parents' mating.arrow_forward
- In humans, the genetic disease cystic fibrosis is caused by a recessive allele (a). The normal (healthy) allele is dominant (A). What is the genotype of someone who has cystic fibrosis? What are the two different genotypes that a healthy person could have? If two people were both heterozygous for the cystic fibrosis gene, what fraction of their children would be likely to have this disease? Hint: Draw a Punnett square to figure it out.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_forwardin humans brown eyes (B) are dominant over blue (b).A brown eye man marries a blue-eyed woman and they have three children , two of whom are brown eyed and one of whom is blue eyed.Draw the punnett square that illustrate this marrage.what is the man's genotype ? what are the genotype of the children?arrow_forward
- In humans, hypertrichosis of the ears is caused by a holandric gene while baldness vs. non-baldness is sex-influenced, controlled by a pair of autosomal alleles, and follows a male-dominant pattern of inheritance. Based on this information, can a normal non-bald daughter have a hypertrichosis bald father? Explain your reasoning and predict the genotypes.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_forwardSkin color in humans is determined by polygenic inheritance, which means the more dominant alleles there are, the darker the skin color will be. A medium-toned skinned woman (AaBb) has a child with another medium-toned skinned man (AaBb). What is the probability of them having a very dark-toned skinned child? (Hint: the genotype is homozygous dominant)arrow_forward
- Colorblindness is inherited as an X-linked recessive trait while pattern baldness is controlled by an autosomal gene that is dominant in males but recessive in females. A colorblind man who is also homozygous for baldness has children with a woman who carries normal genes for both traits. What is the probability that any of their child will be: a. Colorblind, bald male b. Colorblind, normal-haired male c. Female with normal sight and baldarrow_forwardIchthyosis is a rare X-linked recessive disorder that is characterized by scaling of the skin around the neck and lower extremities. A young couple, Bart and Jenny, are expecting a child and are aware there might be a chance that their child could be affected by this disorder. Jenny (the wife) has ichthyosis, but Bart (her husband) is unaffected and completely normal with respect to the allele responsible for this disorder. A. Both Bart and Jenny were Biology majors as undergraduates. Knowing a little about the pattern of X-linked recessive inheritance, Bart and Jenny were concerned when ultrasound revealed that they would be having a son. However, genetic testing performed on the baby shortly after birth revealed that their newborn son, Mark, did not have ichthyosis. Explain how this could be the case, assuming that the gene responsible for ichthyosis is fully penetrant. If non-disjunction occurred, assume it happened in only one of the two parents, and during only one of the two…arrow_forwardColor-blindness (c) is a sex-linked recessive trait, while normal color vision (C) is dominant: If two normal-visioned parents have a color-blind son, what are the parent's genotypes? ~What are the chances that their children will be color-blind?arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Human Anatomy & Physiology (11th Edition)BiologyISBN:9780134580999Author:Elaine N. Marieb, Katja N. HoehnPublisher:PEARSONBiology 2eBiologyISBN:9781947172517Author:Matthew Douglas, Jung Choi, Mary Ann ClarkPublisher:OpenStaxAnatomy & PhysiologyBiologyISBN:9781259398629Author:McKinley, Michael P., O'loughlin, Valerie Dean, Bidle, Theresa StouterPublisher:Mcgraw Hill Education,
- Molecular Biology of the Cell (Sixth Edition)BiologyISBN:9780815344322Author:Bruce Alberts, Alexander D. Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, Peter WalterPublisher:W. W. Norton & CompanyLaboratory Manual For Human Anatomy & PhysiologyBiologyISBN:9781260159363Author:Martin, Terry R., Prentice-craver, CynthiaPublisher:McGraw-Hill Publishing Co.Inquiry Into Life (16th Edition)BiologyISBN:9781260231700Author:Sylvia S. Mader, Michael WindelspechtPublisher:McGraw Hill Education
Human Anatomy & Physiology (11th Edition)
Biology
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:PEARSON
Biology 2e
Biology
ISBN:9781947172517
Author:Matthew Douglas, Jung Choi, Mary Ann Clark
Publisher:OpenStax
Anatomy & Physiology
Biology
ISBN:9781259398629
Author:McKinley, Michael P., O'loughlin, Valerie Dean, Bidle, Theresa Stouter
Publisher:Mcgraw Hill Education,
Molecular Biology of the Cell (Sixth Edition)
Biology
ISBN:9780815344322
Author:Bruce Alberts, Alexander D. Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, Peter Walter
Publisher:W. W. Norton & Company
Laboratory Manual For Human Anatomy & Physiology
Biology
ISBN:9781260159363
Author:Martin, Terry R., Prentice-craver, Cynthia
Publisher:McGraw-Hill Publishing Co.
Inquiry Into Life (16th Edition)
Biology
ISBN:9781260231700
Author:Sylvia S. Mader, Michael Windelspecht
Publisher:McGraw Hill Education
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