ANATOMY & PHYSIOLOGY 4/E PAC 1 SEMESTER
4th Edition
ISBN: 9781265061173
Author: McKinley
Publisher: MCG CUSTOM
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Question
Chapter 29.9, Problem 40WDYL
Summary Introduction
To determine:
The
Concept introduction:
There are some sex-linked traits that are inherited by offspring from their parents. Sex-linked traits are traits expressed by genes on the X or Y chromosomes. These x-linked traits may be recessive or dominant.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Mary and Ron don't have albinism. However, is it possible for them to have a
child with albinism? Explain.
Stephanie has normal color vision. Her husband Chris also has normal color
vision. They have a son that is color blind and a daughter that has normal color
vision. What is the genotype of the mother, father, son and the daughter?
Andy and Anne do not have polydactyl. Is it possible for them to have a child
with polydactyl? Explain.
When examining a pedigree chart, I notice that only males are affected. What
does this tell me about the inheritance pattern?
A man with blood type A marries a woman with blood type B. Their child has
blood type O. What are the genotypes of the parents?
Which of the following genotype(s) must a female child have in order to be color blind?
XNXN XNXn XnXn XNY XnY
(XN represents the normal color vision allele. Xn represents the color-blindness allele. Y represents the Y chromosome, which does not carry the color-vision gene.)
Which of the following genotype(s) must a color-blind male have? Explain your rationale.
XNXN XNXn XnXn XNY XnY
(XN represents the normal color vision allele. Xn represents the color-blindness allele. Y represents the Y chromosome, which does not carry the color-vision gene.)
For a recessive condition, two normal heterozygous individuals have children.
What is the likelihood of their children being affected by this condition?
What is the likelihood of their children being carriers without the condition?
What is the likelihood of their asymptomatic children being carriers?
Suppose that an individual with the condition has children with a heterozygous individual, what is the likelihood of their children being carriers?
Chapter 29 Solutions
ANATOMY & PHYSIOLOGY 4/E PAC 1 SEMESTER
Ch. 29.1 - What distinguishes the pre-embryonic period from...Ch. 29.2 - Prob. 2WDYLCh. 29.2 - Prob. 3WDYLCh. 29.2 - How many cells are present initially in the...Ch. 29.2 - Prob. 5WDYLCh. 29.2 - Prob. 6WDYLCh. 29.2 - Prob. 7WDYLCh. 29.2 - What are the two cell layers of the bilaminar...Ch. 29.2 - Which cell layers give rise to each of the three...Ch. 29.2 - Prob. 10WDYL
Ch. 29.3 - Prob. 11WDYLCh. 29.3 - Prob. 12WDYLCh. 29.3 - Prob. 13WDYLCh. 29.3 - Why is it important for a pregnant woman to...Ch. 29.4 - Prob. 15WDYLCh. 29.5 - Prob. 16WDYLCh. 29.5 - How do estrogen and progesterone act to sustain...Ch. 29.5 - What are the actions of CRH, HPL, oxytocin, and...Ch. 29.5 - Prob. 19WDYLCh. 29.5 - Prob. 20WDYLCh. 29.5 - Prob. 21WDYLCh. 29.5 - Prob. 22WDYLCh. 29.5 - Prob. 23WDYLCh. 29.5 - Prob. 24WDYLCh. 29.5 - Prob. 25WDYLCh. 29.6 - How do progesterone, estrogen, and oxytocin...Ch. 29.6 - Prob. 27WDYLCh. 29.6 - Prob. 28WDYLCh. 29.6 - Prob. 29WDYLCh. 29.6 - Prob. 30WDYLCh. 29.6 - Prob. 31WDYLCh. 29.7 - Prob. 32WDYLCh. 29.7 - Prob. 33WDYLCh. 29.8 - Prob. 34WDYLCh. 29.8 - Prob. 35WDYLCh. 29.8 - How does the positive feedback mechanism in...Ch. 29.8 - Prob. 37WDYLCh. 29.9 - Prob. 38WDYLCh. 29.9 - How does codominant inheritance differ from...Ch. 29.9 - Prob. 40WDYLCh. 29.9 - Prob. 41WDYLCh. 29 - _____ 1. The outer layer of the blastocyst that...Ch. 29 - _____ 2. At about day 3 after fertilization, the...Ch. 29 - During gastrulation, cells from the _____ layer of...Ch. 29 - ______ 4. The cells of the embryoblast...Ch. 29 - _____ 5. Which of the following is not an...Ch. 29 - _____ 6. All of the following cardiovascular...Ch. 29 - _____ 7. After a woman gives birth, what happens...Ch. 29 - _____ 8. Freckles are considered to be a dominant...Ch. 29 - _____ 9. Skin color is a trait that is determined...Ch. 29 - A woman is a carrier for the color-blindness gene,...Ch. 29 - Briefly describe the process of fertilization,...Ch. 29 - List the five regions of the mesoderm, and...Ch. 29 - Explain why teratogens are especially harmful to...Ch. 29 - Describe the differences between the embryonic...Ch. 29 - Prob. 15DYKBCh. 29 - Prob. 16DYKBCh. 29 - Prob. 17DYKBCh. 29 - Describe the various ways by which the mothers...Ch. 29 - Compare and contrast strict dominant-recessive...Ch. 29 - Explain the difference between X-linked recessive...Ch. 29 - Prob. 1CALCh. 29 - Ashley is a 29-year-old pregnant woman who is in...Ch. 29 - Ashley is a 29-year-old pregnant woman who is in...Ch. 29 - Prob. 4CALCh. 29 - Ashley is a 29-year-old pregnant woman who is in...Ch. 29 - Prob. 1CSLCh. 29 - Prob. 2CSLCh. 29 - Prob. 3CSL
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
- Red-green color blindness is inherited as an X-linked recessive (Xc). If a color-blind man marries a woman who is heterozygous for normal vision, what would be the expected phenotypes of their children with reference to this character? In your answer, specify in your phenotype descriptions the gender of the children. (For example, don’t just say 75% of the children would be colorblind – you would instead say 100 % of the daughters would be colorblind and 50% of the sons would be colorblind. Note that this is not a correct answer; it is just to give you an idea of how to explain the correct phenotypes of the cross.)___arrow_forwardIn humans color vision is X-linked, the gene for color vision is located on the X chromosome but is absent on the Y chromosome. Normal color vision (XN) is dominant over colorblindness (Xn). Suppose a colorblind man fathers the children of a woman with genotype XNXN. What is the genotype of the father? What proportion of daughters will be colorblind? What proportion of the sons will be colorblind?arrow_forwardColor blindness is an X-linked recessive disease. A female and a male with normal vision have 4 children. The phenotypes of the children are listed below: 2 Colorblind males, 1 normal vision female, one normal vision male. Given these results, the female must be a carrier for colorblindness. True Falsearrow_forward
- 1. A) Apply the concept of sex linkage to explain why color blindness is more prevalent in men than in women. B) Mary is concerned that she may be a carrier for hemophilia, a sex-linked condition located on the X chromosome. Mary is married to John, who doesn't have hemophilia. Assuming Mary is a carrier, what are the genotype ratios expected for Mary and John's kids (specify for boys and for girls)? C) Mary and John have 2 boys, none of them has hemophilia. Can we use this fact as proof that Mary does not carry the allele for hemophilia? Explain your argument.arrow_forwardA color-blind man marries a woman with normal vision whose father was color-blind. Remember that color-blindness is an X-linked recessive trait. Hint: see figure 12.7 in book. A) What is the probability that their first child will be a color-blind daughter? B) What is the probability that their first son will be color-blind?arrow_forwardA man with X-linked color blindness marries a woman with no history of color blindness in her family. The daughter of this couple marries a normal man, and their daughter also marries a normal man. What is the chance that this last couple will have a child with color blindness? If this couple has already had a child with color blindness, what is the chance that their next child will be color blind?arrow_forward
- In humans, one type of red-green colorblindness (n) is sex-linked and recessive. A) A woman who is a carrier marries a man with normal vision. What is the chance of having color-blind daughters? Color-blind sons? B) A heterozygous woman and a color-blind man marry. What is the chance of having color-blind daughters? Color-blind sons?arrow_forwardA gene that controls the ability to see red and green is located on the X chromosome but not on the Y chromosome. There is a recessive nonfunctional allele for this gene that can cause red-green color blindness if the person possessing it does not also have the dominant normal gene. Consider the case of a carrier mother who is heterozygous for the red-green vision gene and a father who has normal vision. Use XB = normal vision, Xb = color-blind vision. What is the chance the parents would have a color-blind boy? A color-blind girl? What about a girl or boy with normal vision? Redo the Punnett square for a carrier mother (XBXb) and a color-blind father (XbY). Do the chances of having color-blind children change? How?arrow_forwardIf a color blind woman is married to a man with normal vision, what are the chances that the biological daughters from this marriage will be colorblind. What are the chances that the daughters will be carriers?arrow_forward
- Hemophilia 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_forwardAssume that the incidence of an X-linked recessive disorder is 1 in 200 male births. What is the frequency of the mutant allele?arrow_forwardA man who is an achondroplastic dwarf with normal vision marries a color-blind woman of normal height. The man's father was 6 feet tall, and both the woman's parents were of average height. Achondroplastic dwarfism is autosomal dominant, and red-green color blindness is X-linked recessive. a) How many of their daughters might be expected to be color-blind dwarfs? b)What proportion of their sons would be color-blind and of normal height? c)They have a daughter who is a dwarf with normal color vision. What is the probability that she is heterozygous for both genes?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
Animal Communication | Ecology & Environment | Biology | FuseSchool; Author: FuseSchool - Global Education;https://www.youtube.com/watch?v=LsMbn3b1Bis;License: Standard Youtube License