Biology (MindTap Course List)
11th Edition
ISBN: 9781337392938
Author: Eldra Solomon, Charles Martin, Diana W. Martin, Linda R. Berg
Publisher: Cengage Learning
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Question
Chapter 16.3, Problem 3C
Summary Introduction
Concept introduction: Inheritance patterns explain the transmission of a trait in families. They are classified as autosomal or X-linked and dominant or recessive. Based on this, inheritance patterns are autosomal dominant and recessive, and X-linked dominant and recessive.
Expert Solution & Answer
Trending nowThis is a popular solution!
Students have asked these similar questions
2. STATEMENT:
A woman and man both do not have sickle-cell anemia, but both had one parent who
had sickle cell. Sickle-cell is an autosomal (somatic) recessive trait.
a) What is the genotype for the woman, man and each of their parents?
b) This couple unexpectedly is going to have their first child.
i.
What's the probability that their child will have not have sickle cell like the couple?
ii.
What's the probability that the child will have sickle cell like one the grandparents?
Please shows me Punnett square ，so I will know how to solve this problem
AaBbCcDc AaBbCcD Ac
Heading 1 Heading 2
Title
Subtitle
Subtle Em.. Emphasis
Intense E...
Strong
Quote
Int
Paragraph
Styles
4
Genetic Inheritance Patterns
Retinitis pigmentosa (RP) can be autosomal recessive, autosomal dominant, or x-linked.
Apparently the dominant forms are often less severe. Eric's form of RP is Usher's
Syndrome, which is an autosomal recessive inheritance (i.e., you must get a copy of the
defective
carried on one of the chromosomes that determines sex. Usher's Type II is recessive, so
for Eric this means that both his Mom and Dad are carriers of this condition. His
brother, Dirk, does not have any symptoms of RP.
gene from your Mom and one from your Dad). Autosomal means it is not
Question below short answer approach
image you are the genetics counselor, should Eric have children? Imagine he has a
daughter (he has two, but both are adopted). What advice would you give Eric if his wife
was a carrier from a genetics counseling viewpoint? Describe all the possibilities,…
Chapter 16 Solutions
Biology (MindTap Course List)
Ch. 16.1 - Distinguish between karyotyping and pedigree...Ch. 16.1 - Prob. 2LOCh. 16.1 - Prob. 3LOCh. 16.1 - Prob. 1CCh. 16.1 - Prob. 2CCh. 16.1 - Describe two ways in which genome database...Ch. 16.1 - Prob. 4CCh. 16.2 - Explain how nondisjunction in meiosis is...Ch. 16.2 - Distinguish among the following structural...Ch. 16.2 - Prob. 6LO
Ch. 16.2 - VISUALIZE Draw a simple sketch illustrating how...Ch. 16.2 - Prob. 2CCh. 16.2 - Prob. 3CCh. 16.2 - Prob. 4CCh. 16.3 - State whether each of the following genetic...Ch. 16.3 - Which of the following genetic diseases is/are...Ch. 16.3 - Prob. 2CCh. 16.3 - Prob. 3CCh. 16.4 - Briefly discuss the process of gene therapy,...Ch. 16.4 - Prob. 1CCh. 16.5 - State the relative advantages and disadvantages of...Ch. 16.5 - Distinguish between genetic screening programs for...Ch. 16.5 - Prob. 1CCh. 16.5 - Prob. 2CCh. 16.6 - Prob. 11LOCh. 16.6 - Prob. 1CCh. 16.6 - CONNECT To be expressed, an autosomal recessive...Ch. 16.6 - Prob. 3CCh. 16 - Prob. 1TYUCh. 16 - An abnormality in which there is one more or one...Ch. 16 - The failure of chromosomes to separate normally...Ch. 16 - Prob. 4TYUCh. 16 - Prob. 5TYUCh. 16 - Prob. 6TYUCh. 16 - Prob. 7TYUCh. 16 - Prob. 8TYUCh. 16 - Examine the following pedigrees. Which is the most...Ch. 16 - Examine the following pedigrees. Which is the most...Ch. 16 - Prob. 11TYUCh. 16 - SCIENCE, TECHNOLOGY, AND SOCIETY Imagine that you...Ch. 16 - A common belief about human genetics is that an...Ch. 16 - Prob. 14TYUCh. 16 - EVOLUTION LINK Explain some of the evolutionary...
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
- In humans, hemophilia is a sex-linked trait. Females can be normal, carriers, or have the disease. Males will either have the disease or not (but they won’t ever be carriers). X H X H = female, non-hemophilic X H X h = female, carrier X h X h = female, hemophilia X H Y = male, non-hemophilic X h Y= male, hemophiliac a.) Show the cross of a man who has hemophilia with a woman who is a carrier. What is the probability that their children will have the disease? b.) A woman who is a carrier marries a non-hemophilic man. Show the cross. What is the probability that their children will have hemophilia? What sex will a child in the family with hemophilia be? c.) A woman who has hemophilia marries a non-hemophilic man. How many of their children will have hemophilia, and what is their sex?arrow_forward3) State whether each of the following genetic defects is inherited as an autosomal recessive, autosomal dominant, or X-linked recessive trait: phenylketonuria (PKU), sickle cell anemia, cystic fibrosis, Tay-Sachs disease, Huntington’s disease, and hemophilia A.arrow_forwardDoes this individual display any genetic disorders?arrow_forward
- Recessive genetic disorders are more frequent than disorders inherited as dominant because : a) recessive genetic disorders are limited to persons of the same ethnicity c) dominant genetic disorders are never expressed in males d) people carrying dominant genetic disorders always die before birth e ) carriers are not eliminated by the disease before reproductionarrow_forward1. In humans, hemophilia is a sex linked trait. Females can be normal, carriers, or have the disease. Males will have the disease or not (but they won't be ever carriers) XH XH = female, normal XH Xh = female, carrier Xh Xh = female, hemophilic XH Y = male, normal Xh Y = male, hemophilic a) Show the cross of a man who has hemophilia with a woman who is a carrier. b) What is the probability that their children have the diseasearrow_forwardAnswer the following questions about the pedigree shown (below). Assume the trait is rare. • What is the most likely mode of inheritance for this pedigree? autosomal recessive What is the most likely genotype of the following individuals? • 1-2? homozygous recessive • Il-1? homozygous dominant • IV-2? [ Select ] • [V-4? [ Select ] 6대 - 100arrow_forward
- A type of red-green colorblindness is inherited recessively on the X chromosome. A woman who is a carrier had children with a male that is not affected by the disease. Show your answers with the use of a Punnett square • What is the probability (% or likelihood) that a child is affected by the disease? • What is the probability (% or likelihood) that a son is a carrier? (Careful!) • Is there a chance that a girl of the couple is affected by the disease?arrow_forwardWhat is the relationship between individual I-1 and individual III-2? Incidence of Hemophilia homozygous dominant II homozygous recessive III grandfather-granddaughter grandmother-grandson great aunt-nephew mother-sonarrow_forwardMatch the followingarrow_forward
- 6. A man with X-linked colorblindness marries a woman with no history of ibba colorblindness in her family. The daughter of this couple marries a normal man noitenmot and ended up hone daughter, and their daughter also marries a normal man. This mont blast couple has already had a child with color blindness. do sri ni novig A) What is the chance that next child will be color blind? B) What is the chance that this last couple will have an affected daughter? (d #50x²50 (arrow_forward2. Hemophilia is an X linked recessive trait. There is a woman who is a carrier for hemophilia and marries a man with hemophilia. a) Complete the Punnett Square (it is a google drawing so you will have to double click it to go to the drawing and type in and around the square. Hold the CONTROL (or Command) button and press the PERIOD button to write a superscript/exponent.) b) What are the possible genotypes of the children? c) Could any of their children have hemophilia? If so, would the child be male or female? Explain your reasoning.arrow_forward5. A man who is not bald married a non bald female whose mother is bald. A. What is the chance that the couple will have a bald son? B. What is the probability that the couple will have a bald daughter? What is the chance that the couple will have a nonbald daughter? C.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Biology (MindTap Course List)BiologyISBN:9781337392938Author:Eldra Solomon, Charles Martin, Diana W. Martin, Linda R. BergPublisher:Cengage Learning
Human Heredity: Principles and Issues (MindTap Co...BiologyISBN:9781305251052Author:Michael CummingsPublisher:Cengage Learning
Biology (MindTap Course List)
Biology
ISBN:9781337392938
Author:Eldra Solomon, Charles Martin, Diana W. Martin, Linda R. Berg
Publisher:Cengage Learning
Human Heredity: Principles and Issues (MindTap Co...
Biology
ISBN:9781305251052
Author:Michael Cummings
Publisher:Cengage Learning
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