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WorksheetsUnit 4: Geneticorp
Total questions: 90
Worksheet time: 45mins
What is the single cell that is created at fertilization.
zygote
morula
sperm
egg
How many chromosomes does the typical human have?
23
46
52
83
How many PAIRS of chromosomes does the typical human have?
10
23
46
52
What is the name of the complex molecule with a double helix shape?
DNA
chromosome
gene
zygote
A short segment of DNA is called a(n)
gene
zygote
morula
none of these
Which form of cell division results in duplicate cells?
mitosis
meiosis
fertilization
none of these
Which type of cell division occurs with gametes?
mitosis
meiosis
none of these
The sperm and egg cells are called
autosomes
sex chromosomes
gametes
none of these
When the sperm and egg combine to form a single cell, they each are supposed to donate ____ chromosomes.
10
20
23
46
A person's actual genetic makeup is referred to as
genotype
phenotype
none of these
Having brown hair or blue eyes are examples of
genotype
phenotype
mitosis
fertilization
A picture of the number and visual appearance of a person's chromosomes is called a(n)
phenotype
karyotype
mitotic type
none of these
A typical biological male is ____ on the 23rd pair of chromosomes.
XX
XY
XXY
XYY
A typical biological female is ____ on the 23rd pair of chromosomes.
XX
XY
X0
XYY
In typical cases, a mother donates an ___ chromosome on the 23rd pair to her offspring.
X
Y
none of these
True or False: A father can donate an X or Y on the 23rd pair to his offspring.
True
False
True or False: It is the mother's egg that determines biological sex of the offspring.
True
False
True or False: It is the father's sperm that determines the biological sex of the offspring.
True
False
Which condition is also known as Trisomy 21?
Fragile X Syndrome
Klinefelter Syndrome
Turner Syndrome
Down Syndrome
Down Syndrome results from having three copies of chromosome ____.
10
5
21
23
True or False: Maternal age is the number one risk factor for having a child with Down Syndrome.
True
False
At age 35, the rates of a mother having a child with Down Syndrome are
1 in 700
1 in 350
1 in 100
1 in 30
Which disorder includes facial features such as flattened facial profile and small, upward slanting eyes?
Down Syndrome
Klinefelter Syndrome
Turner Syndrome
Cystic Fibrosis
True or False: Symptoms of Down Syndrome include poor muscle tone.
True
False
X-linked chromosome disorders are more common among
males
females
A person who is XXY on the 23rd pair would have which disorder?
Turner Syndrome
Down Syndrome
Klinefelter Syndrome
none of these
Klinefelter Syndrome affects
biological males
biological females
both males and females
Turner Syndrome affects
biological males
biological females
both males and females
True or False: Individuals with Klinefelter Syndrome tend to be shorter than their peers.
True
False
A person with lowered testosterone, wide hips, reduced facial hair, and delayed puberty would most likely be diagnosed with
Klinefelter Syndrome
Turner Syndrome
Fragile X Syndrome
Hemophilia
True or False: Individuals with Klinefelter Syndrome are more likely to experience learning disabilities.
True
False
A person who is X0 on the 23rd pair would be diagnosed with
Klinefelter Syndrome
Turner Syndrome
Fragile X Syndrome
Red-Green Color Blindness
Short stature, a webbed neck, swollen hands and feet, and infertility are typical symptoms of
Turner Syndrome
Fragile X Syndrome
Down Syndrome
Huntington's Disease
True or False: Heart problems are common among individuals with Turner Syndrome.
True
False
Fragile X Syndrome is more common among
males
females
The X chromosome becomes constricted and breaks in
Down Syndrome
Klinefelter Syndrome
Turner Syndrome
none of these
Which condition is caused by mutations of the FMR1 gene?
Fragile X Syndrome
Klinefelter Syndrome
Cystic Fibrosis
Huntington's Disease
Severe intellectual disabilities along with a long, narrow face, prominent jaw and forehead, and flat feet are typical symptoms of
Fragile X Syndrome
Turner Syndrome
Cystic Fibrosis
Tay-Sachs Disease
True or False: Seizures are a possible symptom of Fragile X Syndrome.
True
False
Red-Green Color Blindness affects more
males
females
The mutation for Fragile X Syndrome occurs on which chromosome?
10
12
4
23
The mutation for red-green color blindness occurs on which chromosome?
1
10
17
23
Mutations on genes that make proteins (called OPSIN) in the retina of the eye are responsible for
red-green color blindness
Cystic Fibrosis
Tay-Sachs Disease
none of these
True or False: Individuals with red-green color blindness can only see in black, white, and shades of grey.
True
False
True or False: Cystic Fibrosis is more common among African Americans.
True
False
Mutations on the CFTR gene that are responsible for making a protein that produces sweat, saliva, tears, mucus, and digestive enzymes causes
Cystic Fibrosis
Huntington's Disease
Tay Sachs Disease
Sickle Cell Anemia
Cystic Fibrosis is caused by a mutation on chromosome
3
7
23
11
Which of the following is caused by a mutation on chromosome 7?
Fragile X
Tay Sachs Disease
Huntington's Disease
none of these
Lung transplants are often needed in cases of
Cystic Fibrosis
Huntington's Disease
Down Syndrome
Sickle Cell Anemia
Lung complication are the most common cause of death in cases of
Huntington's Disease
Sickle Cell Anemia
Tay Sachs Disease
Cystic Fibrosis
Insulin production is affected in
Diabetes
Cystic Fibrosis
Tay Sachs Disease
none of these
True or False: Rates of diabetes in childhood has risen in recent years.
True
False
True or False: Diabetes risk involves multiple genes on multiple chromosomes.
True
False
Hemophilia is caused by a mutation on which chromosome pair?
1
7
11
23
Hemophilia is more common among
males
females
Which disorder involves the build-up of a thick sticky mucus in the digestive tract and lungs?
Cystic Fibrosis
Tay Sachs Disease
Diabetes
none of these
Which disorder involves mutations in genes that provide instructions for making proteins called coagulation factors?
Hemophilia
Huntington's Disease
Phenylketonuria
Sickle-Cell Anemia
In individuals with this disorder, bleeding is a serious concern as the blood does not properly clot.
Hemophilia
Fragile X Syndrome
Sickle-Cell Anemia
PKU
Treatment of this disorder involves replacing the missing clotting factors of the blood through an injection.
Huntington's Disease
Diabetes
Tay Sachs Disease
Hemophilia
This disorder is caused by mutations in the HTT gene located on chromosome 4.
Huntington's Disease
Sickle-Cell Anemia
Phenylketonuria
Tay Sachs Disease
Average age of onset of this disorder is typically the 30s or 40s.
Tay Sachs Disease
Sickle Cell Anemia
Huntington's Disease
Cystic Fibrosis
One of the major brain areas that is affected by Huntington's Disease is the
amygdala
basal ganglia
cerebellum
none of these
Typical symptoms of this disorder include depression, irritability, problems with decision making, and motor movements including involuntary movements and poor coordination.
Fragile X Syndrome
Turner Syndrome
Huntington's Disease
Sickle-Cell Anemia
True or False: Blood testing at birth can determine the presence of Phenylketonuria.
True
False
True or False: "Diet for life" is the common treatment for Sickle-Cell Anemia.
True
False
Which disorder is caused by a mutation on chromosome 4?
Phenylketonuria
Sickle-Cell Anemia
Cystic Fibrosis
Huntington's Disease
The inability to process the amino acid phenylalanine is central to
phenylketonuria
sickle-cell anemia
huntington's disease
none of these
Which disorder is caused by a mutation on chromosome 12?
Phenylketonuria
Huntington's Disease
Sickle-Cell Anemia
Cystic Fibrosis
True or False: It is very important for individuals with PKU to avoid protein-based foods.
True
False
What is the typical treatment for an individual with PKU?
a special diet
injections of clotting factors
palliative care
insulin
True or False: If a special diet is not strictly followed for individuals with PKU, severe mental impairment can occur.
True
False
Which disorder is caused by a mutation on chromosome 11?
Huntington's Disease
Tay Sachs Disease
PKU
Sickle-Cell Anemia
Which disorder is caused my mutations in the HBB gene located on chromosome 11?
Sickle-Cell Anemia
Tay Sachs Disease
Cystic Fibrosis
none of these
This disorder results in misshapen red blood cells that die off quicker than normal.
Huntington's Disease
Sickle-Cell Anemia
Tay Sachs Disease
none of these
Delayed growth, vision problems, jaundice, pain, hypertension, heart disease, and stroke are just a few of the possible symptoms with
Fragile X Syndrome
Sickle-Cell Anemia
Turner Syndrome
Klinefelter Syndrome
Which disorder is more common in individuals from easter and central european Jewish descent?
Tay Sachs Disease
Sickle Cell Anemia
Huntington's Disease
none of these
This disorder is caused by mutations in the HEXA gene which is responsible for making an enzyme that acts as a garbage disposal in the nervous system.
Huntington's Disease
Down Syndrome
Sicks-Cell Anemia
none of these
Which disorder affects chromosome 15?
Sickle Cell Anemia
Huntington's Disease
Cystic Fibrosis
Tay Sachs Disease
Symptoms of this disorder include fairly normal development for the first 3-6 months of age and then regression.
Tay Sachs Disease
Huntington's Disease
Klinefelter's Syndrome
Down Syndrome
Typically, death from this disorder occurs early, with an average life expectancy of 5 years old.
Huntington's Disease
Cystic Fibrosis
Tay Sachs Disease
none of these
True or False: There is a cure for Tay Sachs Disease.
True
False
True or False: There is a cure for Huntington's Disease.
True
False
True or False: A lung transplant will cure Cystic Fibrosis.
True
False
Which prenatal testing procedure uses high frequency sound waves to generate a picture of the offspring?
ultrasound
amniocentesis
chorionic villus sampling
noninvasive prenatal testing
True or False: Most pregnant women un the United States will undergo at least one prenatal ultrasound.
True
False
This prenatal testing procedure can be conducted between 15 and 18 weeks gestation and samples the amniotic fluid.
ultrasound
amniocentesis
chorionic villus sampling
none of these
This prenatal testing procedure can be conducted between 9 and 12 weeks gestation and samples the membrane that surrounds the fetus.
ultrasound
amniocentesis
chorionic villus sampling
noninvasive prenatal testing
True or False: It is considered safe to perform the chorionic villus sampling at 4 weeks gestation.
True
False
True or False: There are no risks associated with amniocentesis.
True
False
True or False: Noninvasive prenatal testing is considered to be just as accurate as amniocentesis or chorionic villus sampling.
True
False
