EBK BIOLOGY
5th Edition
ISBN: 9780133996807
Author: Maier
Publisher: PEARSON CUSTOM PUB.(CONSIGNMENT)
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Chapter 8, Problem 10LTB
Summary Introduction
Introduction:
The allele is the form of a single gene present in an organism. The different combination of the alleles determines the genotype and
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Consider a couple: a woman who is homozygous for a recessive mutation that causes X-linked colorblindness, and a man with full color vision (he does not carry a copy of the mutation).
a) What is the probability that a son of this couple will be colorblind?
b) What is the probability that a daughter of the couple will be colorblind?
Color 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
False
In humans, the ABO blood type is under the control of
autosomal multiple alleles. Color blindness is a recessive
X-linked trait. If two parents who are both type A and have
normal vision produce a son who is color blind and is type
O, what is the probability that their next child will be a
female who has normal vision and is type O?
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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
- Analysis of X-Linked Dominant and Recessive Traits A young boy is color-blind. His one brother and five sisters are not. The boy has three maternal uncles and four maternal aunts. None of his uncles children or grandchildren is color-blind. One of the maternal aunts married a color-blind man, and half of her children, both male and female, are color-blind. The other aunts married men who have normal color vision. All their daughters have normal vision, but half of their sons are color-blind. a. Which of the boys four grandparents transmitted the gene for color blindness? b. Are any of the boys aunts or uncles color-blind? c. Is either of the boys parents 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_forwardColorblindness 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_forward
- Hemophilia is an X-linked recessive phenotype. Suppose a man who expresses the hemophilia phenotype has children with a woman who has the normal phenotype (and does not have a family history of hemophilia). If the couple have a son, what are the chances that he will have hemophilia? A) 50% B) 25% C) 0% D) 100%arrow_forwardRed-green color blindness in humans is due to an X- linked recessive gene. Both John and Cathy have normal color vision. Cathy is adopted, and knows nothing about her biological parents. After 10 years of marriage to John, Cathy has given birth to a color-blind daughter and a color-blind son. John filed for divorce, claiming that he is not the father of at least one of the children. Is John justified in his claim of nonpaternity? Yes. He cannot be the father of Cathy's son. b. Yes, He cannot be the father of either child. O c. No. He is the father of both children. d. Yes. He cannot be the father of Cathy's daughter. Next page ge ems: X Inactivation, Nondisjunction, Quiz 3 Sex-linked Traits> Jump to... Pedigree FEB 17 MacBook Air 80 DII DD F1 F2 F3 F4 F5 F6 F7 F8 F9 F10 @ #3 $4 & *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_forward
- Red-green color blindness is an X-linked recessive disorder. A woman with normal vision whose father was colorblind has children with a man with normal color vision. What is the probability that their first child will be colorblind? A) 1/4 B) 1/2 C) 3/4 D) 0 E) 1arrow_forwardColorblindness is an X-linked trait found in humans. What are the chances that a colorblind man will pass it on to his son? Please explain.arrow_forwardA female carrier of the X-linked recessive gene for red-green color blindness will display a phenotype of normal vision. red-green color blindness. XXC.arrow_forward
- An individual with 46, XX genotype is diagnosed with Duchenne-type Muscular Dystrophy, a recessive X-linked disorder. Genetic tests confirm that this individual is a heterozygote for this disorder. Briefly, but specifically, explain how it’s possible that they are showing symptoms of this disorder.arrow_forwardPls answer fastarrow_forwardDuchenne Muscular Dystrophy (DMD) is an X-linked recessive trait. Fill in a Punnett square for a man with DMD and a woman who carries DMD. Then use your Punnett square to answer the following questions: A) What is the probability that one of their daughters will have DMD? ___% B) What is the probability that one of their daughters is a carrier of DMD? ______ % C) What is the probability that one of their sons will have DMD? ______ % D) What is the probability that one of their sons is a carrier of DMD? ______ % E) On which chromosome is the gene for DMD located? _____arrow_forward
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