WorksheetsCategories of Genetic Disorder
Total questions: 50
Worksheet time: 2hrs 40mins
How are the cells of a person with Down syndrome different than those of a person without the disorder?
Down syndrome cells have an extra chromosome
Down syndrome cells are missing a chromosome
Down syndrome cells have codominant alleles
Down syndrome cells have more recessive alleles
What is the purpose of meiosis?
to grow
to heal
to develop
to make reproductive cells
________ is how a trait appears, or is expressed. The part we can see.
Dominance
Genotype
Phenotype
Polygenic Inheritance
The chromosomes inside you exist as ________, one from each of your parents.
Duplicates
Genes
Pairs
Alleles
_________ is when the two alleles of a gene are different. Rr
Heterozygous
Genotype
Phenotype
Homozygous
__________ is when the two alleles of a gene are the same. RR and rr
Heterozygous
Genotype
Phenotype
Homozygous
In __________, uppercase letters represent dominant alleles and lowercase letters represent recessive alleles.
Cells
Genotypes
Genetics
Symbols
Specific characteristic of an individual that can be passed on.
Trait
Asexual Reproduction
Sexual Reproduction
Gamete
The individuals that are heterozygous are ___________, and they are also known as __________________.
male, purebred
female, purebred
male, carriers
female, carriers
If this is a pedigree for colorblindness, what is the genotype of the man in generation 1?
XbXb
XbY
XBYB
XBY
Find the Incorrect statement about Huntington's disease.
It is a progressive neuro-degenerative disorder in humans
It is an autosomal dominant single-gene disease
affected parents have a 50% chance of passing a mutant copy of the huntington gene onto each of their offspring,
Occurs in females only
Which of the following is a recessive disorder?
cystic fibrosis
huntington's disease
down syndrome
hemophilia
If one of your parents has Huntington's, what is your chance of inheriting it?
0%
25%
50%
75%
100%
The Punnett square in Figure 7.1 shows a cross between two parents who are heterozygous for an autosomal genetic disorder caused by a recessive allele.
People with which genotype will have the disorder?
Ss parent
Ss offspring
SS offspring
ss offspring
Down syndrome is characterized by having an extra copy of at least a portion of chromosome 21. Which of the following methods would quickly identify the disorder?
pedigree chart
karyotype
meiosis map
linkage map
Humans with genetic diseases can have a healthy gene inserted into their body. This is called:
Gene therapy
Forensics
DNA fingerprinting
Males are more likely to inherit
a recessive x-linked disorder
a dominant x-linked trait
an autosomal disorder
any dieases
Study the blood cells in the picture below. Describe the genotype for the individual with these types of cells.
homozygous recessive
heterozygous
homozygous dominant
codominant
Why is Down syndrome called trisomy 21
The person has 21 pairs of chromosomes instead of 23.
The person has an abnormal gene on chromosome 21.
The syndrome is caused by having 21 pairs of autosomes.
The syndrome results from an extra chromosome 21.
A man carrying the allele for Huntington’s disease marries a woman who is homozygous recessive for the allele. What is the probability that their offspring will develop Huntington’s disease?
25 percent
50 percent
75 percent
100 percent
You inherit your mitochondrial DNA from your
father
mother
neither
both
