wayground logo

Free Printable Worksheets

NEW

Font size

S
M
L
XL
Worksheets

MTM May 22 Week 4 Genetics

Total questions: 20

Worksheet time: 27mins

Name
Class
Date
1.

When a cytogenetic abnormality is suspected in an infant with multiple congenital anomalies, chromosomes from circulating leukocytes are analyzed. These chromosomes are most condensed and easiest to evaluate in which of the following states?

a)

Anaphase

b)

Interphase

c)

Metaphase

d)

Prophase

e)

Telophase

2.

True or false: Trisomies of sex chromosomes are more likely to survive to gestation than autosomal trisomies.

a)

True

b)

False

3.

The pedigree below tracks the presence of dimples through a family's generation. Having dimples is an autosomal dominant trait. If individual III-3 married a woman who was heterozygous for dimples, what is the  percent chance their children will have dimples?

a)

0%

b)

25%

c)

50%

d)

75%

e)

100%

4.

An experimenter obtains tissue samples from a normal 80-year-old patient and a normal 25-year-old patient and grows fibroblasts from these samples in an in vitro cell culture system. She finds that cells from the older patient stop dividing much sooner than cells from the younger patient. This finding is most likely explained by a difference in which of the following?

a)

circulating levels of cytokines

b)

growth factor activity

c)

hormonal level

d)

oncogene expression

e)

telomere length

5.

Scientists studying aneuploidy identify a substance that inhibits chromosomal separation of chromosome 21 during Meiosis I. If women exposed to this substance become pregnant, their zygotes may have which of the following numbers of chromosomes?

a)

45

b)

43

c)

46

d)

48

e)

44

6.

Are prokaryotic genes polycistronic?

a)

Yes

b)

No

c)

Depends on multiple factors

d)

Only at times

e)

Only during mitosis

7.

The “crossing-over” observed

between chromosomal arms

during human meiosis is better

termed:

a)

Homologous recombination

b)

Polygenic resegregation

c)

Polyclonal diversification

d)

Combinatorial segmentation

e)

Nonrandom assortment

8.

Which of the following statements correctly describes eukaryotic nuclear chromosomal DNA?

a)

Each discontinuous piece making up the chromosomes of eukaryotes is about the same size as each prokaryotic chromosome

b)

Unlike bacterial DNA, no histones are associated with it

c)

It is not replicated semiconservatively

d)

It is a linear and unbranched molecule

e)

It is not associated with a specific membranous organelle

9.

What is the inheritance pattern?

a)

Autosomal Recessive

b)

X-linked Dominant

c)

Mitochondrial

d)

Autosomal Dominant

e)

X-linked Recessive

10.

What is the product of Meiosis I?

a)

An egg or sperm cell

b)

Two diploid cells containing bivalent chromosomes

c)

Four haploid cells containing monovalent chromosomes

d)

Two haploid cells containing bivalent chromosomes

e)

Four diploid cells containing tetravalent chromosomes

11.

As a general rule, new, spontaneous

mutations occurring in a child will occur

more often on the paternal than maternal

chromosomes. Why is this?

a)

DNA repair is weaker in spermatocytes than oocytes

b)

Fathers have shorter life expectancies than mothers

c)

More cell divisions occur in spermatogenesis than oogenesis

d)

Mitochondria are inherited only from mothers

e)

Essential DNA repair genes are found on the X chromosome

12.

This is a pedigree for a family with a history of Cystic  Fibrosis. The III-2 female is affected with CF. What is  the probability that her sister (marked by the arrow) is  a carrier of CF?

a)

50%

b)

75%

c)

33%

d)

25%

e)

66%

13.

If a spontaneous mutation occurs in an

individual, that mutation will only be passed

onto the individual’s offspring if it occurs in

the...

a)

Central Nervous System

b)

Heart

c)

Bone Marrow

d)

Germline

e)

They are in all tissues

14.

What is the inheritance pattern?

a)

Autosomal Recessive

b)

X-linked Dominant

c)

Mitochondrial

d)

Autosomal Dominant

e)

X-linked Recessive

15.

A 24-year-old at 22 weeks gestation presents for prenatal ultrasound testing. Imaging shows a female fetus with a fluid-filled sac near the base of the head. Amniocentesis show the presence of 45 fetal chromosomes. Which of the following conditions is indicated?

a)

Klinefelter Syndrome

b)

Edward’s Syndrome

c)

Down Syndrome

d)

Turner Syndrome

16.

An individual is affected by an autosomal recessive  disease. What is the probability that his unborn sibling  will be a carrier of the AR disease?

a)

50%

b)

75%

c)

33%

d)

25%

e)

66%

17.

A promoter site on DNA

a)

Transcribes repressor

b)

Initiates transcription

c)

Codes for RNA polymerase

d)

Regulates termination

e)

Translates specific proteins

18.

Which disease would follow this inheritance pattern?

a)

Sickle Cell

b)

Fragile X

c)

MELAS

d)

Achondroplasia

e)

Hemophilia

19.

What molecule carries the basic genetic information within a human cell?

a)

Double-helical collagen protein

b)

Double-stranded DNA

c)

A multitude of protein molecules

d)

A multitude of lipid molecules

e)

Linear carbohydrate molecules

20.

The pedigree below tracks Duchenne Muscular Dystrophy (DMD) through several generations.  DMD is an X-linked recessive trait. If individual II-3 has a child with a carrier woman, what is the percent chance that the child will be a daughter with DMD?

a)

0%

b)

25%

c)

50%

d)

75%

e)

100%