Pedigree analysis is necessary when studying human inheritance patterns because . a. humans have more than 20,000 genes b. of ethical problems with experimenting on humans c. inheritance in humans is more complicated than it is in other organisms d. genetic disorders occur only in humans

Pedigree analysis is necessary when studying human inheritance patterns because . a. humans have more than 20,000 genes b. of ethical problems with experimenting on humans c. inheritance in humans is more complicated than it is in other organisms d. genetic disorders occur only in humans

Human Heredity: Principles and Issues (MindTap Course List)

11th Edition

ISBN:9781305251052

Author:Michael Cummings

Publisher:Michael Cummings

Chapter4: Pedigree Analysis In Human Genetics

Section: Chapter Questions

Problem 3CS: Pedigree analysis is a fundamental tool for investigating whether or not a trait is following a...

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. Which of the following terms applies to traits, such as human eye color, that are controlled by more than one gene? A. Codominant B. Polygenic C. Recessive D. Sex-linked
The findings of Mendel were not easily accepted by the scientific community due to: a. he never intended to publish the results b. he used mathematics in analyzing his results c. he did not present the results to the right people d. he had a lot of conflicting results
Which of the following is the definition of the term named Allele? a.Refers to genes that have identical alleles b.Genetic constitution of an organism c.Alternative form of a gene d.Trait expressed in the F1 generation e.Fundamental physical and functional unit of heredity f.Physical expression of traits of an organism
Which of the following is the definition of the term named Genes? a.Refers to genes that have identical alleles b.Genetic constitution of an organism c.Alternative form of a gene d.Trait expressed in the F1 generation e.Fundamental physical and functional unit of heredity f.Physical expression of traits of an organism
When a disease is due to polygenic inheritance, the following is probably true: A. Many factors, both genetic and environmental, contribute to the disease traits. B. It is caused by one gene with a large number of alleles. C. It affects a large number of people. D. It has many different symptoms
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 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?
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?
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. 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?
Which of the following is the definition of the term named Genotype? a.Refers to genes that have identical alleles b.Genetic constitution of an organism c.Alternative form of a gene d.Trait expressed in the F1 generation e.Fundamental physical and functional unit of heredity f.Physical expression of traits of an organism
. The accompanying pedigree concerns a rare inherited dental abnormality, amelogenesis imperfecta.a. What mode of inheritance best accounts for the transmission of this trait? b. Write the genotypes of all family members according to your hypothesis
Which of the following is true regarding understanding the results of genetic testing? A. If the test shows that you have the allele for a genetic disorder, you may be able to reduce your risk of developing that disorder with lifestyle changes. B. If the test shows that you have the allele for a genetic disorder, you will, eventually, show symptoms of that disorder. C. Because we know the functions of all the genes in the human genome, genetic tests can give you complete and accurate information regarding your medical health. D. If the test shows that you do not carry the allele for a particular disorder, there is no chance that you will get that disorder.
Which of the following is the definition of the term named Homozygous? a.Refers to genes that have identical alleles b.Genetic constitution of an organism c.Alternative form of a gene d.Trait expressed in the F1 generation e.Fundamental physical and functional unit of heredity f.Physical expression of traits of an organism