Exam 12: Units of Heredity: Chromosomes and Inheritance

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Nondisjunction in somatic cells can result in aneuploid cells. This may give rise to:

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What percent of males have some degree of color blindness?

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Red-green color blindness is an X-linked recessive trait in humans. A color-blind woman and a man with normal vision have a son. What is the probability that the son is color blind?

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If one of your parents has Huntington disease and is heterozygous for the disorder, you have a 50 percent chance of inheriting the disease.

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Refer to the figure below, and then answer the question that follows. Refer to the figure below, and then answer the question that follows.   -The last members of the Russian Royal Family were executed during the Russian Revolution. Assume the revolution never took place and Alexis, son of Czar Nicholas II and Alexandra, survived and married into the British Royal Family. What is the probability that his children would have hemophilia? What is the probability his children would be carriers for hemophilia? -The last members of the Russian Royal Family were executed during the Russian Revolution. Assume the revolution never took place and Alexis, son of Czar Nicholas II and Alexandra, survived and married into the British Royal Family. What is the probability that his children would have hemophilia? What is the probability his children would be carriers for hemophilia?

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What single attribute determines that a human fetus is male?

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Which condition or disease is caused by aneuploidy?

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Hemophelia is an X-linked recessive disorder. A mother without the allele and a father with the allele have a daughter. The daughter then marries a man with hemophilia. What is the genotype of the daughter? What is the probability that the daughter's children will develop the disease?

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Which of the following is an autosomal recessive disorder?

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If a disease is caused by a dominant allele, it means that a person with the disease:

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A trait such as albinism is seen with equal frequency in males and females. Two people who do not have the trait might have offspring who do have the trait, at a frequency of approximately one in four. What can you conclude about the inheritance of this trait?

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A carrier for a genetic disorder will pass the allele to all of their offspring.

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A person must have two alleles for hemoglobin S in order to suffer from sickle-cell anemia.

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Cri-du-chat syndrome babies are mentally challenged and have an abnormal larynx that makes sounds like the cry of a cat. This disorder is due to a/an:

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What do hemophilia, Duchenne muscular dystrophy, and red-green color blindness have in common?

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A pedigree is a representation of:

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What is a recessive disorder?

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Refer to the figure below, and then answer the question that follows. Refer to the figure below, and then answer the question that follows.   -Nondisjunction in meiosis gives rise to gametes with abnormal chromosome numbers. Which event is likely to produce a higher percentage of abnormal gametes? -Nondisjunction in meiosis gives rise to gametes with abnormal chromosome numbers. Which event is likely to produce a higher percentage of abnormal gametes?

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In humans, aneuploidy is fairly common yet goes largely unrecognized as a genetic problem. This is because:

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You have studied the presence of a trait in the members of three generations of a family. With this information, you constructed a ________ to track how the trait was passed down through the generations.

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