Biology: The Unity and Diversity of Life (MindTap Course List)
14th Edition
ISBN: 9781305073951
Author: Cecie Starr, Ralph Taggart, Christine Evers, Lisa Starr
Publisher: Cengage Learning
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Chapter 14, Problem 2GP
Does the
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Chapter 14 Solutions
Biology: The Unity and Diversity of Life (MindTap Course List)
Ch. 14 - Constructing a pedigree is particularly useful...Ch. 14 - Prob. 2SQCh. 14 - Prob. 3SQCh. 14 - Prob. 4SQCh. 14 - Prob. 5SQCh. 14 - A trait that is present in a male child but not in...Ch. 14 - Color blindness is a case of ______ inheritance....Ch. 14 - A female child inherits one X chromosome from her...Ch. 14 - Prob. 1DAACh. 14 - Prob. 2DAA
Ch. 14 - Prob. 3DAACh. 14 - Prob. 9SQCh. 14 - Expression of the SRY gene on the Y chromosome...Ch. 14 - Prob. 11SQCh. 14 - Prob. 12SQCh. 14 - Prob. 13SQCh. 14 - Prob. 14SQCh. 14 - Match the chromosome terms appropriately. ____...Ch. 14 - Prob. 1GPCh. 14 - Does the phenotype indicated by the red circles...Ch. 14 - Human females have two X chromosomes (XX); males...Ch. 14 - A mutated allele responsible for Marfan syndrome...Ch. 14 - The somatic cells of most individuals with Down...Ch. 14 - Mutations in the genes for clotting factor VIII...
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An allele responsible for Marfan syndrome Section 13.4 is inherited in an autosomal dominant pattern. What is the chance that a child will inherit the allele if one parent does not carry it and the other is heterozygous?
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The following pedigree shows the pattern of inheritance of red-green color blindness in a family. Females are shown as circles and males as squares; the squares or circles of individuals affected by the trait are filled in black. What is the chance that a son of the third-generation female indicated by the arrow will be color blind if the father is not color blind? If he is color blind?
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What is a carrier of a genetic trait?
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Could an individual with blood type O (genotype ii) be a legitimate child of parents in which one parent had blood type A and the other parent had blood type B?
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Could the pedigree in Figure 2-31 be explained as an autosomal dominant disorder? Explain.
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What is the specific mode of inheritance shown in this pedigree?
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How can you tell if a pedigree is autosomal dominant or recessive?
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When examining a human pedigree, what features do you look forto distinguish between X-linked recessive inheritance and autosomal recessive inheritance? How would you distinguish X-linkeddominant inheritance from autosomal dominant inheritance in ahuman pedigree?
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In a cross between an individual with Huntington disease and an unaffected individual, what are the chances their progeny will have the disease, considering that it is a dominant trait?
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which mode of inheritance does this trait show (autosomal recessive, autosomal dominant, X-linked recessive, X-linked dominant, Y-linked, or mitochondrial).
And why?
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What is the difference between an autosomal dominant andautosomal recessive pattern of inheritance?
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Is this pedigree Sex-linked recessive, Autosomal recessive, or Both? Explain?.
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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