Human Biology Custom Edition
11th Edition
ISBN: 9781337631532
Author: Cecie Starr, Beverly McMillan
Publisher: Cengage Learning
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Chapter 20, Problem 4CT
Summary Introduction
To explain: Whether a trait that appears in males only provided good evidence that it is caused by Y-linked allele.
Introduction: Y-linked traits denote that a gene for a particular trait is located on the Y-chromosome. Sex influences traits denote that a gene for a particular trait is located on autosome but is influenced by the sex of that individual.
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Color blindness is caused by an X-linked recessive allele that is rare in humans. Suppose two parents have normal color vision and color-blind fathers. What is the chance that their second son will have normal vision?.
pleasee answer item no. 4, 5, and 6
Could a woman with the X-linked color-blind trait have a son without colorblindness? Use a Punnett square to explain your answer.
Chapter 20 Solutions
Human Biology Custom Edition
Ch. 20 - Prob. 1RQCh. 20 - What is a carrier of a genetic trait?Ch. 20 - What evidence indicates that a trait is coded by a...Ch. 20 - Prob. 4RQCh. 20 - Explain what nondisjunction is, and give two...Ch. 20 - _______ segregate during ______. a. Homologues;...Ch. 20 - Prob. 2SQCh. 20 - Genes on the same chromosome tend to stay together...Ch. 20 - Prob. 4SQCh. 20 - A chromosomes structure can be altered by _______....
Ch. 20 - Nondisjunction can be caused by ________. a....Ch. 20 - A gamete affected by nondisjunction could have...Ch. 20 - Genetic disorders can be caused by __________. a....Ch. 20 - A person who is a carrier for a genetic trait...Ch. 20 - Prob. 10SQCh. 20 - If a couple has six boys, what is the probability...Ch. 20 - Human sex chromosomes are XX for females and XY...Ch. 20 - People with Down syndrome have an extra copy of...Ch. 20 - Prob. 4CTCh. 20 - Prob. 5CTCh. 20 - About 4 percent of people of Northern European...Ch. 20 - The following pedigree shows the pattern of...
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- 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. Predict the genotype of the man. (XH = normal; Xh= hemophiliac) * a. XH Y b. XHXh c. XhXh d. Xh Yarrow_forwardDoing genetic analysis it is determined that two parents are heterozygous for two separate unlinked recessive traits (i.e., both parents are heterozygous for both loci). Given this genetic information, what is the probability of their having a child which is homozygous recessive for both traits?arrow_forwardCan anyone step by step explain this question？arrow_forward
- Assume that a disease called Disease B is known to be x-linked but we don’t know if it’s a dominant or recessive allele that causes it. Looking at how common this disease is in males and females would give us the answer. How?arrow_forwardHemophilia 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%arrow_forwardIn certain species of flies, eye color is controlled by sim-·ple dominance by a single pair of alleles. A red-eyed fly was crossed with a white-eyed fly, both of whose parents had white eyes. All of their offspring (both female and male) had red eyes.a. Which is dominant, the allele for red eyesor the allele for white eyes?b. What is the genotype of the white-eyed parents?c. If the white-eyed parent was mated with one of the red-eyed offspring, what phenotypic ratio wouldyou expect regarding eye color?arrow_forward
- what is a genotype and what is a phenotype? Explain how these concepts relate to the concepts of dominant and recessive genesarrow_forwardWould you expect dominant X-linked traits to affect women as often as men? Explain your answer.arrow_forwardplease answer item no.4, 5, and 6 pleaseee.arrow_forward
- In humans, color blindness is a sex-linked recessive trait. A female who is a carrier (XBXb) for color blindness has children with a male with normal vision (XBY). Make a Punnett Square to help you answer the questions. What are the chances of their children being color blind? What are the chances of their children being ‘carriers’ for color blindness?arrow_forwardA tortoiseshell cat, such as the cat pictured, is likely to be female. Why do tortoiseshell coats occur primarily in female cats? Testosterone suppresses the tortoiseshell gene in males, so tortoiseshell coats appear more often in females, who have less testosterone than males. Tortoiseshell coloring is an X-linked recessive trait, so females with two X chromosomes are more likely to express the trait than males. One of a female's two X chromosomes is randomly inactivated in each cell, so each cell may express different alleles. O The X chromosome is disabled in males, so a tortoiseshell coat, which is an X-linked recessive trait, does not occur in males.arrow_forwardWhen crossing a normal hen with a short-legged rooster, all the normal hens and all the short-legged hens came out. Subsequently, the F2 is carried out and it is obtained that half of the roosters and half of the hens come out short legged. Try to explain these results, assign the alleles.arrow_forward
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