Mindtap Biology, 1 Term (6 Months) Printed Access Card For Solomon/martin/martin/berg's Biology, 11th
11th Edition
ISBN: 9781337393096
Author: Eldra Solomon, Charles Martin, Diana W. Martin, Linda R. Berg
Publisher: Cengage Learning
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Chapter 16, Problem 14TYU
Summary Introduction
To determine: Whether a chromosome deletion is equivalent to a frame shift mutation.
Concept introduction: Chromosomal disorders are inherited conditions that occur due to abnormalities in chromosomes during meiosis. They are classified as numerical abnormalities in chromosomes and structural abnormalities.
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Is a chromosome deletion equivalent to a frameshift mutation ? Why orwhy not?
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Chapter 16 Solutions
Mindtap Biology, 1 Term (6 Months) Printed Access Card For Solomon/martin/martin/berg's Biology, 11th
Ch. 16.1 - Distinguish between karyotyping and pedigree...Ch. 16.1 - Prob. 2LOCh. 16.1 - Prob. 3LOCh. 16.1 - Prob. 1CCh. 16.1 - Prob. 2CCh. 16.1 - Describe two ways in which genome database...Ch. 16.1 - Prob. 4CCh. 16.2 - Explain how nondisjunction in meiosis is...Ch. 16.2 - Distinguish among the following structural...Ch. 16.2 - Prob. 6LO
Ch. 16.2 - VISUALIZE Draw a simple sketch illustrating how...Ch. 16.2 - Prob. 2CCh. 16.2 - Prob. 3CCh. 16.2 - Prob. 4CCh. 16.3 - State whether each of the following genetic...Ch. 16.3 - Which of the following genetic diseases is/are...Ch. 16.3 - Prob. 2CCh. 16.3 - Prob. 3CCh. 16.4 - Briefly discuss the process of gene therapy,...Ch. 16.4 - Prob. 1CCh. 16.5 - State the relative advantages and disadvantages of...Ch. 16.5 - Distinguish between genetic screening programs for...Ch. 16.5 - Prob. 1CCh. 16.5 - Prob. 2CCh. 16.6 - Prob. 11LOCh. 16.6 - Prob. 1CCh. 16.6 - CONNECT To be expressed, an autosomal recessive...Ch. 16.6 - Prob. 3CCh. 16 - Prob. 1TYUCh. 16 - An abnormality in which there is one more or one...Ch. 16 - The failure of chromosomes to separate normally...Ch. 16 - Prob. 4TYUCh. 16 - Prob. 5TYUCh. 16 - Prob. 6TYUCh. 16 - Prob. 7TYUCh. 16 - Prob. 8TYUCh. 16 - Examine the following pedigrees. Which is the most...Ch. 16 - Examine the following pedigrees. Which is the most...Ch. 16 - Prob. 11TYUCh. 16 - SCIENCE, TECHNOLOGY, AND SOCIETY Imagine that you...Ch. 16 - A common belief about human genetics is that an...Ch. 16 - Prob. 14TYUCh. 16 - EVOLUTION LINK Explain some of the evolutionary...
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Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.Similar questions
- What is chromosome 12 deletion effects?arrow_forwardWhat types of chromosome mutations are required to change this chromosome into the following chromosomes? (In some cases, more than one chromosome mutation may be required.) Q. A B • C F E D Garrow_forwardWhy is chromosome 21 Down syndrome?arrow_forward
- The genes that codes for the creation of certain blood groups are located on chromosome "XGp22.3", chromosome "12p12.3", chromosome "2q14.3", and so on. What is this chromosome terminology? What does it mean?arrow_forwardWhich types of chromosome mutations a. increase the amount of genetic material in a particular chromosome? b. increase the amount of genetic material in all chromosomes? c. decrease the amount of genetic material in a particular chromosome? d. change the position of DNA sequences in a single chromosome without changing the amount of genetic material? e. move DNA from one chromosome to a nonhomologous chromosome?arrow_forwardColchicine is a chemical mutagen that inhibits the spindle formation and prevents anaphase, which retains the cell’s single restitution nucleus (doubled chromosome number). Suppose that an onion (2n=16) is subjected to three consecutive rounds of colchicine treatment, what will be the resulting chromosome number of the treated onion?arrow_forward
- why would a mutation complex 1 usually not result in immediate death ? And while blocking complex IV can result in immediate death ?arrow_forwardThe work of McClintock showed that the presence of a transposoncan create a mutable site or locus that is subject to frequent chromosomebreakage. Why do you think a transposon creates a mutable site? If chromosome breakage occurs, do you think the transposon has moved somewhere else? How would you experimentally determine if it has?arrow_forwardA plant geneticist was examining the inversion mutation XI 501 in barley where a segment of DNA is removed, flipped, and reinserted in reverse order. The original protein functioned to assist in the separation of daughter cells during meiosis. A model of the initiation of normal protein translation is shown in the diagram. The action of the mutation is shown in orange. Using the model, which of the following predicts how the XI 501 mutation affects the protein produced? A - It creates a protein with the order of amino acids reversed, causing the protein to fold backward, reducing pollen functionality. B - It creates a nonsense protein that does not function in the cell, causing the cell to use energy to remove the proteins, reducing pollen fertility. C - It creates a protein that terminates at the mutation, causing the pollen to carry more than one copy of the genetic material in each granule. D - It creates a protein with half the amino acids correct and half reversed, reducing…arrow_forward
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