Exam 8: Variation in Chromosome Structure and Number

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Homologous genes within a species are called paralogs.

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True

A loss of an internal piece of a chromosome is called a __________.

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C

The majority of autosomal aneuploid conditions are lethal, but sex chromosome aneuploids are usually not lethal.

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_______ is a drug that is used to experimentally produce polyploidy in organisms.

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An inversion heterozygote contains

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Klinefelter and Turner syndromes are examples of

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Which of the following is not an example of euploidy?

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The effects of a deficiency on an organism is dependent on the size of the deletion and the importance of the missing genetic material to the organism.

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Given the following sequence of genes on a chromosome, determine what change in chromosome structure occurred. (the * indicates the centromere) before A B C D * E F G H After A C D * E F G H

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A diploid organism has a total of 36 chromosomes. Assuming all possible chromosome combinations are viable, if a mutant tetraploid version of this organism was created how many chromosomes would it have? If a mutant version of this organism was monosomic for chromosome 9 how many chomosomes would it have?

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A _______ translocation represents when a piece of one chromosome is attached to another chromosome.

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The production of gene families, such as the globin genes is the result of ________.

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Edward and Patau syndromes are examples of __________.

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Given the following sequence of genes on a chromosome, determine what change in chromosome structure occurred. (the * indicates the centromere) before A B C D * E F G H After A B C D * E F E F G H

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A wholphin is a rare hybrid animal born from mating a female bottlenose dolphin with a male false killer whale. Wholphins are diploid. Interestingly, wholphins are fertile. What can you conclude from the fact that wholphins are fertile?

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Hemophilia A is an X-linked blood clotting disorder. A normal man and a woman with hemophilia A have a child with Turner Syndrome. This child does not have hemophilia. In whom did non-disjunction occur? In meiosis I or meiosis II?

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Translocations and inversions represent a change in the total genetic material of a chromosome.

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A translocation cross may occur in an individual that has a(n)

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Human genetic diseases such a Cri-du-chat, Angelman syndrome and Prader-Willi syndrome are the result of which type of chromosomal change?

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Which algebraic expression would be used to denote a trisomic organism?

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