BIOLOGY:THE ESSENTIALS (LL) W/CONNECT
3rd Edition
ISBN: 9781260670929
Author: Hoefnagels
Publisher: MCG CUSTOM
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Chapter 10, Problem 1SL
Review Burning Question 10.10, which describes the inheritance pattern of the
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Chapter 10 Solutions
BIOLOGY:THE ESSENTIALS (LL) W/CONNECT
Ch. 10.1 - How are chromosomes, DNA, genes, and alleles...Ch. 10.1 - Prob. 2MCCh. 10.2 - Why did Gregor Mendel choose pea plants as his...Ch. 10.2 - Distinguish between dominant and recessive;...Ch. 10.3 - Prob. 1MCCh. 10.3 - How are Punnett squares helpful in following the...Ch. 10.3 - Prob. 3MCCh. 10.3 - Prob. 4MCCh. 10.4 - What is a dihybrid cross, and what is the...Ch. 10.4 - Prob. 2MC
Ch. 10.4 - Prob. 3MCCh. 10.5 - How do the patterns of inheritance differ for...Ch. 10.5 - What is the difference between recombinant and...Ch. 10.5 - Prob. 3MCCh. 10.6 - Prob. 1MCCh. 10.6 - What is pleiotropy?Ch. 10.6 - Prob. 3MCCh. 10.6 - Prob. 4MCCh. 10.7 - Prob. 1MCCh. 10.7 - Prob. 2MCCh. 10.7 - Prob. 3MCCh. 10.8 - How are pedigrees helpful in determining a...Ch. 10.8 - Prob. 2MCCh. 10.9 - Prob. 1MCCh. 10.9 - Prob. 2MCCh. 10 - In the list of four terms below, which term is the...Ch. 10 - Prob. 2MCQCh. 10 - Prob. 3MCQCh. 10 - Prob. 4MCQCh. 10 - Prob. 5MCQCh. 10 - Prob. 6MCQCh. 10 - Prob. 1WIOCh. 10 - List three genes mentioned in this chapter or not...Ch. 10 - Prob. 3WIOCh. 10 - Prob. 4WIOCh. 10 - Prob. 5WIOCh. 10 - Explain how each of the following appears to...Ch. 10 - Prob. 8WIOCh. 10 - Calico cats have large patches of orange and...Ch. 10 - Prob. 10WIOCh. 10 - Review Burning Question 10.10, which describes the...Ch. 10 - Prob. 1PITCh. 10 - Analyze the concept map and then explain the...Ch. 10 - Add meiosis, gametes, mutations, incomplete...Ch. 10 - In rose bushes, red flowers FF or Ff are dominant...Ch. 10 - In Mexican hairless dogs, a dominant allele...Ch. 10 - Prob. 3GPCh. 10 - Two lizards have green skin and large dewlaps...Ch. 10 - A fern with a genotype AA Bb Cc dd Ee mates with...Ch. 10 - In Fraggles, males are genotype XY and females are...
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- Pedigree analysis is a fundamental tool for investigating whether or not a trait is following a Mendelian pattern of inheritance. It can also be used to help identify individuals within a family who may be at risk for the trait. Adam and Sarah, a young couple of Eastern European Jewish ancestry, went to a genetic counselor because they were planning a family and wanted to know what their chances were for having a child with a genetic condition. The genetic counselor took a detailed family history from both of them and discovered several traits in their respective families. Sarahs maternal family history is suggestive of an autosomal dominant pattern of cancer predisposition to breast and ovarian cancer because of the young ages at which her mother and grandmother were diagnosed with their cancers. If a mutant allele that predisposed to breast and ovarian cancer was inherited in Sarahs family, she, her sister, and any of her own future children could be at risk for inheriting this mutation. The counselor told her that genetic testing is available that may help determine if this mutant allele is present in her family members. Adams paternal family history has a very strong pattern of early onset heart disease. An autosomal dominant condition known as familial hypercholesterolemia may be responsible for the large number of deaths from heart disease. As with hereditary breast and ovarian cancer, genetic testing is available to see if Adam carries the mutant allele. Testing will give the couple more information about the chances that their children could inherit this mutation. Adam had a first cousin who died from Tay-Sachs disease (TSD), a fatal autosomal recessive condition most commonly found in people of Eastern European Jewish descent. Because TSD is a recessively inherited disorder, both of his cousins parents must have been heterozygous carriers of the mutant allele. If that is the case, Adams father could be a carrier as well. If Adams father carries the mutant TSD allele, it is possible that Adam inherited this mutation. Because Sarah is also of Eastern European Jewish ancestry, she could also be a carrier of the gene, even though no one in her family has been affected with TSD. If Adam and Sarah are both carriers, each of their children would have a 25% chance of being afflicted with TSD. A simple blood test performed on both Sarah and Adam could determine whether they are carriers of this mutation. Would you decide to have a child if the test results said that you carry the mutation for breast and ovarian cancer? The heart disease mutation? The TSD mutation? The heart disease and the mutant alleles?arrow_forwardPedigree analysis is a fundamental tool for investigating whether or not a trait is following a Mendelian pattern of inheritance. It can also be used to help identify individuals within a family who may be at risk for the trait. Adam and Sarah, a young couple of Eastern European Jewish ancestry, went to a genetic counselor because they were planning a family and wanted to know what their chances were for having a child with a genetic condition. The genetic counselor took a detailed family history from both of them and discovered several traits in their respective families. Sarahs maternal family history is suggestive of an autosomal dominant pattern of cancer predisposition to breast and ovarian cancer because of the young ages at which her mother and grandmother were diagnosed with their cancers. If a mutant allele that predisposed to breast and ovarian cancer was inherited in Sarahs family, she, her sister, and any of her own future children could be at risk for inheriting this mutation. The counselor told her that genetic testing is available that may help determine if this mutant allele is present in her family members. Adams paternal family history has a very strong pattern of early onset heart disease. An autosomal dominant condition known as familial hypercholesterolemia may be responsible for the large number of deaths from heart disease. As with hereditary breast and ovarian cancer, genetic testing is available to see if Adam carries the mutant allele. Testing will give the couple more information about the chances that their children could inherit this mutation. Adam had a first cousin who died from Tay-Sachs disease (TSD), a fatal autosomal recessive condition most commonly found in people of Eastern European Jewish descent. Because TSD is a recessively inherited disorder, both of his cousins parents must have been heterozygous carriers of the mutant allele. If that is the case, Adams father could be a carrier as well. If Adams father carries the mutant TSD allele, it is possible that Adam inherited this mutation. Because Sarah is also of Eastern European Jewish ancestry, she could also be a carrier of the gene, even though no one in her family has been affected with TSD. If Adam and Sarah are both carriers, each of their children would have a 25% chance of being afflicted with TSD. A simple blood test performed on both Sarah and Adam could determine whether they are carriers of this mutation. Would you want to know the results of the cancer, heart disease, and TSD tests if you were Sarah and Adam? Is it their responsibility as potential parents to gather this type of information before they decide to have a child?arrow_forwardPedigree analysis is a fundamental tool for investigating whether or not a trait is following a Mendelian pattern of inheritance. It can also be used to help identify individuals within a family who may be at risk for the trait. Adam and Sarah, a young couple of Eastern European Jewish ancestry, went to a genetic counselor because they were planning a family and wanted to know what their chances were for having a child with a genetic condition. The genetic counselor took a detailed family history from both of them and discovered several traits in their respective families. Sarahs maternal family history is suggestive of an autosomal dominant pattern of cancer predisposition to breast and ovarian cancer because of the young ages at which her mother and grandmother were diagnosed with their cancers. If a mutant allele that predisposed to breast and ovarian cancer was inherited in Sarahs family, she, her sister, and any of her own future children could be at risk for inheriting this mutation. The counselor told her that genetic testing is available that may help determine if this mutant allele is present in her family members. Adams paternal family history has a very strong pattern of early onset heart disease. An autosomal dominant condition known as familial hypercholesterolemia may be responsible for the large number of deaths from heart disease. As with hereditary breast and ovarian cancer, genetic testing is available to see if Adam carries the mutant allele. Testing will give the couple more information about the chances that their children could inherit this mutation. Adam had a first cousin who died from Tay-Sachs disease (TSD), a fatal autosomal recessive condition most commonly found in people of Eastern European Jewish descent. Because TSD is a recessively inherited disorder, both of his cousins parents must have been heterozygous carriers of the mutant allele. If that is the case, Adams father could be a carrier as well. If Adams father carries the mutant TSD allele, it is possible that Adam inherited this mutation. Because Sarah is also of Eastern European Jewish ancestry, she could also be a carrier of the gene, even though no one in her family has been affected with TSD. If Adam and Sarah are both carriers, each of their children would have a 25% chance of being afflicted with TSD. A simple blood test performed on both Sarah and Adam could determine whether they are carriers of this mutation. If Sarah carries the mutant cancer allele and Adam carries the mutant heart disease allele, what is the chance that they would have a child who is free of both diseases? Are these good odds?arrow_forward
- As a physician, you deliver a baby with protruding heels and clenched fists with the second and fifth fingers over-lapping the third and fourth fingers. a. What genetic disorder do you suspect the baby has? b. How do you confirm your suspicion?arrow_forwardWill insurance companies be able to deny coverage or even treatment of illnesses that can now be revealed through in utero genetic testing?arrow_forwardGenetics affects many aspects of our lives. Identify three ways genetics affects your life or the life of a family member or friend. The effects can be regularly encountered or can be one time only or occasional.arrow_forward
- Which three factors are crucial in the diagnosis of genetic defects in the fetal stage? What do you think weighs the most?arrow_forwardWhat is the most common symptom in a genetic disorder and why? Do all people exhibit this symptom of a genetic disorder?arrow_forwardWhat is an example of why genetic testing is done on prospective parents?arrow_forward
- INTRODUCTION: Pedigrees are symbolic representations of family relationships and the transmission of inherited traits. For researchers, families are tools; the bigger the family, the easier it is to discern modes of inheritance. Pedigrees apply Mendel’s laws to predict the recurrence risks of inherited conditions. INSTRUCTION: Discuss the pedigree using appropriate terms.arrow_forwardSome geneticists, notably Nobel Prize-winner Dr. Herman J. Muller, have proposed that sperm banks solicit donations of sperm cells from carefully selected men whose lives had shown unusual mental, emotional, or physical gifts. Couples would then be able to select the genetic material of their choice and thereby produce a child endowed with the hereditary characteristics that matched their ideals. Evaluate the morality of this proposal with Kant's ethics.arrow_forwardWhat is pedigree Analysis? What are its use or uses?arrow_forward
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