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Genetic Assessment Quiz B

Total questions: 15

Worksheet time: 8mins

Name
Class
Date
1.

Karyotyping reveals characteristic structure of a chromosome

a)

True

b)

False

2.

Sickle cell anemia is commonly found among Caucasians

a)

True

b)

False

3.

Thalassemia is a blood disorder that causes the body to have less hemoglobin

a)

True

b)

False

4.

Tay Sach's disease occurs most often in people of Jewish ancestry.

a)

True

b)

False

5.

It is a diagnostic test wherein amniotic fluid is aspirated to check for chromosomal abnormality

a)

Chronic Villi Sampling

b)

FISH

c)

Amniocentesis

d)

Duplication test

6.

If gene markers for both parents match, it can result to a medical condition of the offspring.

a)

True

b)

False

7.

Chorionic villi sampling can be done as early as 10th-13th week AOG.

a)

True

b)

False

8.

An allele codes for a specific gene

a)

True

b)

False

9.

A genotype is the "outward expression of a gene"

a)

True

b)

False

10.

The dominant trait is the one usually expressed.

a)

True

b)

False

11.

Humans have 23 chromosomes pair, 22 sex chromosomes and 1 autosome

a)

True

b)

False

12.

In autosomal dominant disorder, only a single disease gene is needed to have the disease

a)

True

b)

False

13.

Most X-linked inherited disorders are dominant in nature.

a)

True

b)

False

14.

Mothers with X-linked disorder will have sons with 50% having the disorder and daughters 50% carriers.

a)

True

b)

False

15.

Fathers with an X-linked disorder will not have sons that will inherit the disorder but daughters will be carriers.

a)

True

b)

False