Mindtap Biology, 1 Term (6 Months) Printed Access Card For Solomon/martin/martin/berg's Biology, 11th
11th Edition
ISBN: 9781337393096
Author: Eldra Solomon, Charles Martin, Diana W. Martin, Linda R. Berg
Publisher: Cengage Learning
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Chapter 16, Problem 8TYU
Summary Introduction
Concept introduction: The inheritance patterns for the inheritance of traits are autosomal dominant or recessive, or sex-linked. The traits due to the genes on autosomes are inherited in a simple Mendelian pattern; they can be dominant or recessive. An autosomal dominant trait appears in individuals with a dominant allele, whether they are homozygous or heterozygous. An autosomal recessive trait appears in individuals that are homozygous for the recessive allele.
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Chapter 16 Solutions
Mindtap Biology, 1 Term (6 Months) Printed Access Card For Solomon/martin/martin/berg's Biology, 11th
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...
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- Albinism, lack of pigmentation in humans, results from an autosomal recessive gene (a). Two parents with normal pigmentation have an albino child. (a) What is the probability that their next child will be albino? (b) What is the probability that their next child will be an albino girl? (c) What is the probability that their next three children will be albino?arrow_forwardHemophilia is an X-linked recessive disease. A hemophilic man marries a woman who is not a carrier of the disease. (a) Draw a Punnett square showing the genotypes of their children. (b) What are the chances that their daughters will be carriers of the disease? (c) What percentage of their children are likely to have the disease?arrow_forwarda) Identify and describe 5 different types of genetic inheritance.(b) In humans, glucose-6-phosphate dehydrogenase deficiency is a recessive X-linkedtrait. Describe the inheritance of this disease, including an example of the possibleoutcomes of:(i) An affected mother and an unaffected father having children. (ii) An affected father and a homozygous unaffected mother having childrenarrow_forward
- TO င် ၅ဝပ် တွင် တွင် ၏ ဝ DO (A) The blue trait is inherited as an autosomal recessive trait which means that affected individuals have copies of a mutant gene. (B) Indicate which individuals are carriers of the "blue" gene by placing the letters Bb next to their symbol. (C) What is the relationship of the parents of the "blue" children? (D) What is the probability that the unaffected siblings of the "blue" children are carriers for the "blue" trait? (E) What warning does marrying close relatives does this illustrate?arrow_forwardA particular person is said to be a carrier of a genetic trait. What does this tell you about their phenotype? (a) They physically show the trait. (b) They physically show the trait more than a noncarrier would show the trait.(c) They are almost normal but show an intermediate phenotype for the trait. (d) They are completely normal and do not physically show the trait.arrow_forwardIf two genes are located on different chromosome types then (a) the mother’s genotype will determine the phenotype of the son (b) the genes will not be inherited independently (c) parents that are heterozygous for both genes will produce children displaying a 9:3:3:1 ratio (d) one gene will mask or hide the effect of the other (e) none of the abovearrow_forward
- Suppose that a grandfather, mother, and son all have the same homozygous dominant genotype for a gene that controls facial hair growth. The grandfather and son have thick beards, but the mother has no significant facial hair. What type of non-Mendelian inheritance is this? O a) Sex-influenced inheritance Ob) Sex-limited inheritance Oc) Onset of genetic expression O d) X-linked dominant inheritancearrow_forwardIf an allele must be present on both the maternal and paternal chromosomes to affect the phenotype, the allele is said to be, (a) dominant. (c) complementary. (b) recessive. (d) heterozygous.arrow_forwardAlbinism in humans is inherited as a simple recessive trait. For the following families, determine the genotypes of the parents and offspring. (When two alternative genotypes are possible, list both.) (a) Two normal parents have five children, four normal and one albino. (b) A normal male and an albino female have six children, all normal. (c) A normal male and an albino female have six children, three normal and three albino. (d) Construct a pedigree of the families in (b) and (c). Assume that one of the normal children in (b) and one of the albino children in (c) become the parents of eight children. Add these children to the pedigree, predicting their phenotypes (normal or albino).arrow_forward
- Now assume that the pedigree shown in question 1 shows the inheritance of a rare genetic disease. a) The disease is most likely autosomal dominant b) The disease is most likely autosomal recessive c) The disease is equally likely to be either autosomal dominant or autosomal recessive, but cannot be x-linked d) Cannot be determined from the information givenarrow_forwardSuppose that a grandfather, mother, and son all have the same homozygous dominant genotype for a gene that controls facial hair growth. The grandfather and son have thick beards, but the mother has no significant facial hair. What type of hon-Mendelian inheritance is this? Oa) Sex-influenced inheritance O b) Sex-limited inheritance Oc) Onset of genetic expression D d) X-linked dominant inheritancearrow_forwardCould the trait indicated in the pedigree above be caused by an autosomal gene? Hint: consider each type of autosomal inheritance and see if it could explain the inheritance of the trait. a) Yes, an autosomal dominant gene could explain this trait. b) Yes, an autosomal recessive gene could explain this trait. c) No, an autosomal gene could not account for this pedigree. d) Yes, A and B are true.arrow_forward
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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