
Chromosomal Mutations Lesson
Presentation
•
Biology
•
9th - 12th Grade
•
Easy
+1
Standards-aligned
Bailee Conner
Used 4+ times
FREE Resource
8 Slides • 14 Questions
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2
3
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8
Multiple Choice
What is nondisjunction?
A chromosomal mutation involving the loss of a segment of a chromosome
A condition in which an individual has an extra copy of a specific chromosome
A genetic disorder characterized by intellectual disability and distinct facial features
A genetic event during cell division when chromosomes fail to separate properly
9
Multiple Choice
What is trisomy?
A chromosomal mutation involving the loss of a segment of a chromosome
A condition in which an individual has an extra copy of a specific chromosome
A genetic disorder characterized by intellectual disability and distinct facial features
A genetic event during cell division when chromosomes fail to separate properly
10
Multiple Choice
What is monosomy?
A condition in which an individual has an extra copy of a specific chromosome
A genetic disorder characterized by intellectual disability and distinct facial features
A genetic event during cell division when chromosomes fail to separate properly
A condition in which an individual is missing one copy of a specific chromosome
11
Multiple Choice
What is Down syndrome?
A genetic event during cell division when chromosomes fail to separate properly
A genetic disorder characterized by intellectual disability and distinct facial features
A condition in which an individual has an extra copy of a specific chromosome
A chromosomal mutation involving the loss of a segment of a chromosome
12
Multiple Choice
What is Turner syndrome?
A chromosomal mutation involving the loss of a segment of a chromosome
A genetic disorder in which an individual is born with a single X chromosome
A genetic disorder characterized by intellectual disability and distinct facial features
A condition in which an individual has an extra copy of a specific chromosome
13
Multiple Choice
What is Klinefelter syndrome?
A genetic disorder characterized by intellectual disability and distinct facial features
A genetic disorder in which an individual is born with a single X chromosome
A chromosomal mutation involving the loss of a segment of a chromosome
A genetic disorder characterized by the presence of an extra X chromosome in males
14
Multiple Choice
A mutation is defined as:
A change in the cell's structure
Anything that changes in an embryo
Any change in the physical features of a human
A change in the DNA sequence
15
Multiple Choice
By looking at the chromosomes how can you tell that this person is biologically female?
Because there are two X chromosomes
Because there are more chromosomes than in a male
16
Multiple Choice
This is known as Edwards Syndrome, can you identify the chromosomal mutation?
Chromosomes 1 and 2 are bent
There is no Y chromosome
This persons chromosomes are normal
There are 3 of chromosomes 18
17
Multiple Choice
______________________________________ is a type of chromosomal mutation when part of the chromosome breaks off and attaches to another chromosome.
duplication
translocation
subtraction
deletion
18
Multiple Choice
This type of chromosomal mutation produces an extra copy of all or part of the chromosome:
multiplication
replication
duplication
inversion
19
Multiple Choice
If part of the chromosome is turned around in the opposite direction this is called:
inversion
translocation
deletion
duplication
20
Multiple Choice
In some cases this condition of having extra sets of chromosomes can be beneficial, such as in certain plants that are stronger and larger as a result.
polyploidy
point mutation
frameshift mutation
inversion
21
Multiple Choice
Mutations can be beneficial because they increase genetic _____________________ and can make the individual and species more likely to survive.
diseases
complications
disorders
diversity
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Explanation Slide...
Turner syndrome is a genetic disorder where an individual is born with a single X chromosome, making it the correct choice.
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