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Chromosomal Mutations Lesson

Chromosomal Mutations Lesson

Assessment

Presentation

•

Biology

•

9th - 12th Grade

•

Easy

•
NGSS
HS-LS3-2, HS-LS3-1, HS-LS4-2

+1

Standards-aligned

Created by

Bailee Conner

Used 4+ times

FREE Resource

8 Slides • 14 Questions

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Multiple Choice

What is nondisjunction?

1

A chromosomal mutation involving the loss of a segment of a chromosome

2

A condition in which an individual has an extra copy of a specific chromosome

3

A genetic disorder characterized by intellectual disability and distinct facial features

4

A genetic event during cell division when chromosomes fail to separate properly

9

Multiple Choice

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What is trisomy?

1

A chromosomal mutation involving the loss of a segment of a chromosome

2

A condition in which an individual has an extra copy of a specific chromosome

3

A genetic disorder characterized by intellectual disability and distinct facial features

4

A genetic event during cell division when chromosomes fail to separate properly

10

Multiple Choice

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What is monosomy?

1

A condition in which an individual has an extra copy of a specific chromosome

2

A genetic disorder characterized by intellectual disability and distinct facial features

3

A genetic event during cell division when chromosomes fail to separate properly

4

A condition in which an individual is missing one copy of a specific chromosome

11

Multiple Choice

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What is Down syndrome?

1

A genetic event during cell division when chromosomes fail to separate properly

2

A genetic disorder characterized by intellectual disability and distinct facial features

3

A condition in which an individual has an extra copy of a specific chromosome

4

A chromosomal mutation involving the loss of a segment of a chromosome

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Multiple Choice

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What is Turner syndrome?

1

A chromosomal mutation involving the loss of a segment of a chromosome

2

A genetic disorder in which an individual is born with a single X chromosome

3

A genetic disorder characterized by intellectual disability and distinct facial features

4

A condition in which an individual has an extra copy of a specific chromosome

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Multiple Choice

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What is Klinefelter syndrome?

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A genetic disorder characterized by intellectual disability and distinct facial features

2

A genetic disorder in which an individual is born with a single X chromosome

3

A chromosomal mutation involving the loss of a segment of a chromosome

4

A genetic disorder characterized by the presence of an extra X chromosome in males

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Multiple Choice

A mutation is defined as:

1

A change in the cell's structure

2

Anything that changes in an embryo

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Any change in the physical features of a human

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A change in the DNA sequence

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Multiple Choice

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By looking at the chromosomes how can you tell that this person is biologically female?

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Because there are two X chromosomes

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Because there are more chromosomes than in a male

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Multiple Choice

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This is known as Edwards Syndrome, can you identify the chromosomal mutation?

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Chromosomes 1 and 2 are bent

2

There is no Y chromosome

3

This persons chromosomes are normal

4

There are 3 of chromosomes 18

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Multiple Choice

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______________________________________ is a type of chromosomal mutation when part of the chromosome breaks off and attaches to another chromosome.

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duplication

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translocation

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subtraction

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deletion

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Multiple Choice

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This type of chromosomal mutation produces an extra copy of all or part of the chromosome:

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multiplication

2

replication

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duplication

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inversion

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Multiple Choice

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If part of the chromosome is turned around in the opposite direction this is called:

1

inversion

2

translocation

3

deletion

4

duplication

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Multiple Choice

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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.

1

polyploidy

2

point mutation

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frameshift mutation

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inversion

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Multiple Choice

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Mutations can be beneficial because they increase genetic _____________________ and can make the individual and species more likely to survive.

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diseases

2

complications

3

disorders

4

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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