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TEST AP101-1
Questions:
Test Duration:
Reading Time:
90 Multiple-Choice Questions
110 minutes
10 minutes
INSTRUCTION:
Only Bilingual Dictionaries allowed, NO NOTES. This test consists of one part, ninety (90)
multiple choice questions (numbers 1 to 90) to be answered on the computer answer
2. If two genes are located on the same chromosome, then the traits are often inherited
together and the genes considered
A.
B.
C.
D.
carried
linked
lost
inserted
3. Genetic variation in the offspring results from all but one of the following.
A. random fertilization
B. meiosis
C. mitosis
D. crossing over
4. The genetic information may change due to environment insults resulting in
A.
B.
C.
D.
mutations
crossing over
dominant expression
independent assortment
A child whose mother has type AB blood and father O could have
type A or type B or type O
type A only
type A or type B
type B only
11.
If one parent is heterozygous for Huntington's disease, what is the child's chance
for having the disease?
A. 25%
B. 50%
C. 100%
D. 0%
12.
A.
B.
C.
D.
13.
A.
B.
C.
D.
14.
A.
B.
C.
D.
15.
Amniocentesis ():
A.
B.
C.
D.
16.
A.
B.
C.
D.
17.
19.
A.
B.
C.
D.
20.
Sunlight is an environmental factor that may influence the expression of some
genes.
A. this statement is false
B. this would only happen in males
C. this would only in females
D. this statement is true
21.
A.
B.
C.
D.
22.
Which of the following correctly matches each of the types of inheritance with the
phenotype ()?
A. polygenic; height
B. sex-linked; Tay-Sachs disease
C. dominant-recessive; hemophilia
D. both B and C
23.
Which of the following genetic diseases are not inherited as simple autosomal
recessive traits ()?
A. cystic fibrosis
B. albinism
C. hemophilia
D. Tay-Sachs
24.
A.
B.
C.
D.
25.
Which of the following is not true of genetics?
A. a gene is a segment of a DNA molecule
B. each chromosome contains one or more molecules of DNA
5
A.
B.
C.
D.
27.
A normally pigmented female (Pp) and albino man (pp) are planning on having
children. What is the % chance of them having another albino child?
A. 50%
B. 25%
C. 0%
D. 100%
28.
A.
B.
C.
D.
A end of chromosome which indicates the age or state of each cell is ():
centromere
telomere
intron
exon
29.
A man has been diagnosed with Huntingtons disease, an autosomal dominant
trait. Assuming that his wife is normal, what is the likelihood his son will develop
Huntingtons later in life.
A. 50%
B. 25%
C. 0%
D. 100%
30.
A.
B.
C.
D.
31.
A.
B.
C.
D.
32.
Which of the following is not true of Huntingtons disease (HD)?
A. is progressive neurodegenerative disease
6
35.
A.
B.
C.
D.
Transcription is:
the copying of DNA during the S phase of cell division
the conversion of mRNA to protein
the conversion of DNA to mRNA
the conversion of DNA to protein
36.
Which of the following would you expect to see in an autosomal dominant
pedigree?
A. the trait appearing in every generation
B. the trait appearing in only males
C. the trait skipping generations
D. the trait appearing to follow a knights move pattern
37.
A.
B.
C.
D.
38.
A father has type O blood and the mothers genotype is AO. What percentage of
their offspring will have type A blood?
A. 25%
B. 50%
C. 75%
D. 100%
39.
Which of the following incorrectly matches the mode of genetic expression with
the correct characteristic?
A. polygenic inheritance; traits depend on several different chromosomes
B. dominant-recessive inheritance; one allele can mask the other allele
C. incomplete dominance; heterozygote has a phenotype that is intermediate
between the homozygous dominant and recessive phenotypes
D. sex-linked inheritance; one form is Y-linked, and the other is X-linked
7
44.
A.
B.
C.
D.
45.
A.
B.
C.
D.
46.
What type of allele will be expressed if both dominant and recessive alleles are
present for a given trait?
A. dominant
B. recessive
C. autosomal
D. co-dominant
47.
A.
B.
C.
D.
49.
A person who inherits the A and the O blood type alleles will possess which blood
type?
A. O
B. AB
C. A
D. B
50.
Which of the following incorrectly matches the number of chromosomes with the
cell type?
A. gametes, 2n
B. haploid cells, n
C. diploid cells, 2n
D. both B and C
51.
A.
B.
C.
D.
52.
A.
B.
C.
D.
53.
Abnormal colour vision is 20 times more common in men than women because
most cases are caused by an abnormal ()
A. dominant gene on the Y chromosome
B. recessive gene on the Y chromosome
C. dominant gene on the X chromosome
D. recessive gene on the X chromosome
54.
A.
B.
C.
D.
55.
A.
B.
C.
D.
57.
There are 64 possible codons for 20 amino acids which helps protect against any
error in protein synthesis. This is called ():
A. redundancy in genetic codes
B. complementary genetic codes
C. chiasma in genetic codes
D. independent assortment of genetic codes
58.
Traits that display continuous phenotypic variation are usually determined by this
form of inheritance.
A. polygenic inheritance
B. sex-linked inheritance
C. dominant-recessive inheritance
D. incomplete dominance
59.
What is the probability of having a child with a recessive trait if both parents are
heterozygous for the trait?
A. 75%
B. 50%
C. 100%
D. 25%
60.
A.
B.
C.
D.
61.
Heterozygous individuals that can pass on recessive, abnormal conditions are
referred to as:
A. recessively compromised
B. zygotic
C. phenotypically challenged
D. carriers
62.
A.
B.
C.
D.
Genes that are located on the same chromosome are said to be:
syncopated
linked
crossed
tied
63.
A.
B.
C.
D.
66.
A.
B.
C.
D.
67.
A person with a missing Y chromosome (i.e., 45, X) will
disorder is called
.
A. show female characteristics; Turner syndrome
B. be sterile, but show male characteristics; Klinefelter syndrome
C. show both male and female characteristics; Down syndrome
D. show male characteristics; Klinefelter syndrome
, and this
68.
A.
B.
C.
D.
69.
A.
B.
C.
D.
70.
A.
B.
C.
D.
71.
A.
B.
C.
D.
If the allele for brown hair was represented as "B": would mean that:
brown hair was a recessive trait
the gene for brown hair is carried on the paternal chromosome
brown hair was a dominant trait
the gene for brown hair is carried on the maternal chromosome
72.
The number of different gametes that can be produced in a male, based on
independent assortment alone, equals ():
A.
23
11
B.
C.
23
D.
246
73.
A.
B.
C.
D.
74.
Heterozygous parents who have had one child with a recessive disease will have a
___ chance of having their second child being born with the same recessive disease.
A. 12.5%
B. 75%
C. 25%
D. 50%
75.
Which of the following is true?
A. it is possible to detect heterozygous carriers of Tay-Sachs, cystic fibrosis, and
sickle cell anaemia
B. females inherit more sex-linked traits than males
C. continuous phenotypic variation is characteristic of incomplete dominance or
intermediate inheritance
D. the two sex chromosomes are considered autosomes
76.
A.
B.
C.
77.
When the two alleles controlling a trait are different, the individual is _____ for the
trait.
A. recessive
B. heterozygous
C. homozygous
D. dominant
78.
A.
B.
C.
D.
79.
A.
B.
C.
D.
An allele that is able to mask the expression of its partner allele is said to be:
homozygous
recessive
heterozygous
dominant
Which of the following is not an example of aneuploidy ()?
Tay-sachs disease
Klinefelter syndrome
Turner syndrome
Downs syndrome
12
82.
A.
B.
C.
D.
Which of the following is not one of the three basic levels of gene controls?
mutations
protein-coding genes
epigenetic marks
small RNAs
83.
In an individual human, all body cells (except sex cells) divide into identical
daughter cells by mitosis. Which of the following statement best described the reason
why body cells are different in structure and functions even though they have the
same DNA?
A. because a different cell is located in a different location
B. because different chemicals are present in each body regions
C. because different types of cells turn on or off specific genes
D. because different types of cells have different mutations on specific genes
84.
A.
B.
C.
D.
85.
A.
B.
C.
D.
86.
A.
B.
C.
D.
Linked genes:
are usually recessive
are usually on the same chromosome
are usually dominant
are usually on different chromosomes
87.
Use the following information to solve the problem using a Punnett square.
Assume that the dominant "B" allele encodes brown eyes and the recessive "b" allele
encodes blue eyes.
An individual with the genotype bb has children with an individual of the genotype
Bb.
What is the percent chance that they would have children with blue eyes?
A. 25%
B. 50%
13
89.
A.
B.
C.
90.
A.
B.
C.
D.
14