Exam 18: Patterns of Inheritance
Exam 1: Biology: The Scientific Study of Life40 Questions
Exam 2: Evolution and the Diversity of Life42 Questions
Exam 3: Evolutionary Change and Adaptation43 Questions
Exam 4: Organisms in Their Habitat39 Questions
Exam 5: Ecological Interactions Among Organisms41 Questions
Exam 6: Animal Structure and Function45 Questions
Exam 7: Animal Growth and Development44 Questions
Exam 8: Animal Feeding and Digestion42 Questions
Exam 9: Animal Respiration, Circulation, and Metabolism46 Questions
Exam 10: Animal Sensory Perception, Integration, and Movement41 Questions
Exam 11: Animal Mating and Reproduction44 Questions
Exam 12: Plant Growth, Structure, and Function55 Questions
Exam 13: Plants Functioning in Their Habitat56 Questions
Exam 14: Plant Reproduction56 Questions
Exam 15: The Biology of Fungi56 Questions
Exam 16: Physical Cycles and the Biosphere50 Questions
Exam 17: Preserving Biodiversity Through Conservation Biology51 Questions
Exam 18: Patterns of Inheritance44 Questions
Exam 19: Biotechnology and Genetics38 Questions
Exam 20: Infectious Diseases and the Bodys Responses43 Questions
Exam 21: The Biology of Chronic Disease40 Questions
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All of the following are true about this image EXCEPT:

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D
Assuming a widow's peak is a dominant trait, the father would be __________.

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A
This figure shows chromosomes lined up at the equator of the cell. Which stage of division does this represent?

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B
Muscular dystrophy is a group of inherited disorders that lead to increasing muscle cell loss and thus muscle weakness over time. There are many different types of muscular dystrophy. Symptoms can vary, although all involve muscle weakness. Duchenne muscular dystrophy (DMD) is a recessive X-linked form that leads to muscle degeneration and death usually by age 25. Symptoms begin before age 5 and include low endurance and difficulties standing. As the condition progresses, muscle tissue is replaced with adipose and other types of connective tissue. Abnormal bone development and some neurobehavioral and learning disabilities may also occur. DMD occurs as a result of a mutation in a single gene on the X chromosome. This gene codes for a particular protein, dystrophin, which plays a major role in the structure of muscle cells. The protein formed by the mutated gene is nonfunctional, and the absence of a functional protein eventually leads to cell death. Bone and adipose are examples of __________.
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Joshua is colorblind, but neither of his parents are colorblind. Which of the following is the most likely scenario?
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Muscular dystrophy is a group of inherited disorders that lead to increasing muscle cell loss and thus muscle weakness over time. There are many different types of muscular dystrophy. Symptoms can vary, although all involve muscle weakness. Duchenne muscular dystrophy (DMD) is a recessive X-linked form that leads to muscle degeneration and death usually by age 25. Symptoms begin before age 5 and include low endurance and difficulties standing. As the condition progresses, muscle tissue is replaced with adipose and other types of connective tissue. Abnormal bone development and some neurobehavioral and learning disabilities may also occur. DMD occurs as a result of a mutation in a single gene on the X chromosome. This gene codes for a particular protein, dystrophin, which plays a major role in the structure of muscle cells. The protein formed by the mutated gene is nonfunctional, and the absence of a functional protein eventually leads to cell death. Other types of muscular dystrophy arise due to mutations on chromosomes other than the sex chromosomes. The common name for these other chromosomes is __________.
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The gene that codes for the number of fingers on the human hand has two alleles-five fingers and six fingers. The letters F and f are used to represent this trait. Having five fingers is the recessive trait. A woman has six fingers, but one of her parents has five fingers. She marries a man who has five fingers. Which of the following represents gametes that could be produced by the woman?
(Multiple Choice)
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Assuming a cleft chin is dominant, the father's genotype would be __________.

(Multiple Choice)
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Muscular dystrophy is a group of inherited disorders that lead to increasing muscle cell loss and thus muscle weakness over time. There are many different types of muscular dystrophy. Symptoms can vary, although all involve muscle weakness. Duchenne muscular dystrophy (DMD) is a recessive X-linked form that leads to muscle degeneration and death usually by age 25. Symptoms begin before age 5 and include low endurance and difficulties standing. As the condition progresses, muscle tissue is replaced with adipose and other types of connective tissue. Abnormal bone development and some neurobehavioral and learning disabilities may also occur. DMD occurs as a result of a mutation in a single gene on the X chromosome. This gene codes for a particular protein, dystrophin, which plays a major role in the structure of muscle cells. The protein formed by the mutated gene is nonfunctional, and the absence of a functional protein eventually leads to cell death. Who is more likely to suffer from DMD?
(Multiple Choice)
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Jack has type O blood and his mother has type A blood. His father could have any of the following blood types EXCEPT
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The gene that codes for the number of fingers on the human hand has two alleles-five fingers and six fingers. The letters F and f are used to represent this trait. Having five fingers is the recessive trait. A woman has six fingers, but one of her parents has five fingers. She marries a man who has five fingers. What is the probability that they will have a child who is homozygous dominant for this trait?
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Domestication results from __________ selection, rather than __________ selection.
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Green seed color is dominant over yellow seed color. What is the genotype of a plant that produces gametes with yellow seed color?
(Multiple Choice)
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Muscular dystrophy is a group of inherited disorders that lead to increasing muscle cell loss and thus muscle weakness over time. There are many different types of muscular dystrophy. Symptoms can vary, although all involve muscle weakness. Duchenne muscular dystrophy (DMD) is a recessive X-linked form that leads to muscle degeneration and death usually by age 25. Symptoms begin before age 5 and include low endurance and difficulties standing. As the condition progresses, muscle tissue is replaced with adipose and other types of connective tissue. Abnormal bone development and some neurobehavioral and learning disabilities may also occur. DMD occurs as a result of a mutation in a single gene on the X chromosome. This gene codes for a particular protein, dystrophin, which plays a major role in the structure of muscle cells. The protein formed by the mutated gene is nonfunctional, and the absence of a functional protein eventually leads to cell death. The introduction mentions three out of four major tissue types found in animals. The tissue that is not mentioned is __________ tissue.
(Multiple Choice)
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Muscular dystrophy is a group of inherited disorders that lead to increasing muscle cell loss and thus muscle weakness over time. There are many different types of muscular dystrophy. Symptoms can vary, although all involve muscle weakness. Duchenne muscular dystrophy (DMD) is a recessive X-linked form that leads to muscle degeneration and death usually by age 25. Symptoms begin before age 5 and include low endurance and difficulties standing. As the condition progresses, muscle tissue is replaced with adipose and other types of connective tissue. Abnormal bone development and some neurobehavioral and learning disabilities may also occur. DMD occurs as a result of a mutation in a single gene on the X chromosome. This gene codes for a particular protein, dystrophin, which plays a major role in the structure of muscle cells. The protein formed by the mutated gene is nonfunctional, and the absence of a functional protein eventually leads to cell death. The single gene mutation associated with DMD leads to various symptoms that include bone growth, muscles, and behaviors. This is an example of __________.
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__________ are the functional units of heredity, and they code for specific __________.
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Muscular dystrophy is a group of inherited disorders that lead to increasing muscle cell loss and thus muscle weakness over time. There are many different types of muscular dystrophy. Symptoms can vary, although all involve muscle weakness. Duchenne muscular dystrophy (DMD) is a recessive X-linked form that leads to muscle degeneration and death usually by age 25. Symptoms begin before age 5 and include low endurance and difficulties standing. As the condition progresses, muscle tissue is replaced with adipose and other types of connective tissue. Abnormal bone development and some neurobehavioral and learning disabilities may also occur. DMD occurs as a result of a mutation in a single gene on the X chromosome. This gene codes for a particular protein, dystrophin, which plays a major role in the structure of muscle cells. The protein formed by the mutated gene is nonfunctional, and the absence of a functional protein eventually leads to cell death. A woman who is a carrier for DMD marries a man who does not have the disease. What is the probability that they will have a boy with DMD?
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Traits such as weight and height that tend to vary along a continuum are typically __________.
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The common ancestor of orangutans, gorillas, chimpanzees, and humans existed approximately _____ million years ago.

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