Understand Key Concepts
A normal human diploid zygote contains
23 chromosomes.
46 chromosomes.
44 chromosomes.
XXY chromosomes.
A chart that traces the inheritance of a trait in a family is called a(n)
pedigree.
karyotype.
genome.
autosome.
An example of a trait that is determined by multiple alleles is
cystic fibrosis.
ABO blood groups.
Down syndrome.
colorblindness.
What is the difference between autosomes and sex chromosomes?
Is it possible for a person with blood type alleles IA and IB to have blood type A? Explain your answer. (Refer to Figure 14–5).
Predict What are the possible genotypes of the parents of a male child who is colorblind?
Design an Experiment Fruit fly sex is determined by X and Y chromosomes, just as it is in humans. Researchers suspect that a certain disease is caused by a recessive allele in a gene located on the X chromosome in fruit flies. Design an experiment to test this hypothesis.
Understand Key Concepts
A mutation involving a change in a single DNA base pair
will definitely result in a genetic disease.
will have no effect on the organism's phenotype.
will produce a positive change.
may have an effect on the organism's phenotype.
Cystic fibrosis is caused by
nondisjunction of an autosome.
a change of three base pairs in DNA.
nondisjunction of a sex chromosome.
deletion of an entire gene from a chromosome.
Malaria is a disease caused by a
gene mutation.
defect in red blood cells.
bacterium found in water.
parasite carried by mosquitoes.
Analyze the human karyotype below. Identify the chromosomal disorder that it shows.
What is a chromosomal disorder?
Describe two sex-chromosome disorders.
Infer Can a genetic counselor use a karyotype to identify a carrier of cystic fibrosis? Explain.