Biology
12th Edition
ISBN: 9780134813448
Author: Audesirk, Teresa, Gerald, Byers, Bruce E.
Publisher: Pearson,
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Chapter 11.8, Problem 3CYL
Summary Introduction
To explain: The reason why sex-linked recessive disorders mainly affect males and tend to skip generations.
Introduction: The genetic disorder causes a disease in an individual due to mutation in a sequence of the genome. It can also be caused due to the inversion of genes, deletion, translocation or aneuploidy, nullisomy, and trisomy or polysomy of the chromosomes.
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Describe a recessive epistatic gene.
Compare and contrast the inheritance of recessive, dominant, and sex-linked genetic disorders.
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Chapter 11 Solutions
Biology
Ch. 11.1 - describe the relationships among chromosomes,...Ch. 11.1 - Prob. 2CYLCh. 11.2 - distinguish between self-fertilization and...Ch. 11.2 - Prob. 2CYLCh. 11.3 - Prob. 1TCCh. 11.3 - Prob. 1CSCCh. 11.3 - describe the pattern of inheritance of a trait...Ch. 11.3 - Prob. 2CYLCh. 11.3 - Prob. 3CYLCh. 11.4 - Can the genotype of a plant grown from a smooth,...
Ch. 11.4 - Prob. 2TCCh. 11.4 - Prob. 1CYLCh. 11.4 - Prob. 2CYLCh. 11.4 - Prob. 3CYLCh. 11.5 - Prob. 1TCCh. 11.5 - Prob. 1CSCCh. 11.5 - Prob. 1HYEWCh. 11.5 - Prob. 1CYLCh. 11.5 - Prob. 2CYLCh. 11.6 - describe how the patterns of inheritance differ...Ch. 11.7 - If a color-deficient woman and a man with normal...Ch. 11.7 - Prob. 1CYLCh. 11.7 - explain why most sex-linked traits are controlled...Ch. 11.7 - describe the pattern of inheritance of sex-linked...Ch. 11.8 - Prob. 1TCCh. 11.8 - use pedigrees to determine the pattern of...Ch. 11.8 - Prob. 2CYLCh. 11.8 - Prob. 3CYLCh. 11.8 - Prob. 2TCCh. 11.8 - Prob. 1CTCh. 11 - Prob. 1MCCh. 11 - Prob. 2MCCh. 11 - Independent assortment means that a. two genes on...Ch. 11 - Prob. 4MCCh. 11 - Prob. 5MCCh. 11 - An organism is described as Rr, with red coloring....Ch. 11 - Prob. 2FIBCh. 11 - Prob. 3FIBCh. 11 - Genes that are present on one sex chromosome but...Ch. 11 - Prob. 5FIBCh. 11 - Define the following terms: gene, allele,...Ch. 11 - Prob. 2RQCh. 11 - Prob. 3RQCh. 11 - Prob. 4RQCh. 11 - Prob. 5RQCh. 11 - Prob. 6RQCh. 11 - Prob. 1ACCh. 11 - Prob. 2ACCh. 11 - In certain cattle, hair color can be red...Ch. 11 - In the edible pea, tall (T) is dominant to short...Ch. 11 - Prob. 3GPCh. 11 - Prob. 4GPCh. 11 - Prob. 5GP
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- Explain the Autosomal Recessive Disorders ?arrow_forwardColor-blindness (c) is a sex-linked recessive trait, while normal color vision (C) is dominant: If two normal-visioned parents have a color-blind son, what are the parent's genotypes? ~What are the chances that their children will be color-blind?arrow_forwardGive three examples of recessive epistasis?arrow_forward
- Explain why X-linked recessive traits are often more common in males but X-linked dominant traits are often more common in females.arrow_forwardFor 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?arrow_forwardOne form of the bleeding disorder known as von Willebrand disease is an autosomal recessive disease. A man who is a carrier marries a woman who is also a carrier of the disease. (a) What percentage of their children are likely to have a disease phenotype? (b) What percentage of their children are likely to have a normal phenotype? (c) What percentage of their children are likely to be carriers of the disease?arrow_forward
- What is recessive epistasis?arrow_forwardIn a multigenerational study of a family, 8% of the males and 8% of the females have red hair. What may be the cause of this? A)Autosomal inheritance B)Environmental influence C)Sex-linked inheritance D)Non-somatic inheritancearrow_forwardIn genetics, what does a genotype of Hh signify? Choose 1 answer: Choose 1 answer: (Choice A) A Homozygous; two dominant alleles (Choice B) B Homozygous; two recessive alleles (Choice C) C Heterozygous; one dominant allele and one recessive allele (Choice D) D Homozygous; one dominant allele and one recessive allelearrow_forward
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