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Given that these two gene loci are very closely linked, the phenotypic ratio in the F2 generation should be closest to


A) 1 brown eye, heavy wing veins: 2 red eye, thin wing veins: 1 brown eye, thin wing veins
B) 1 brown eye, thin wing veins: 2 red eye, thin wing veins: 1 red eye, heavy wing veins
C) 3 red eye, thin wing veins: 1 brown eye, heavy wing veins
D) 1 brown eye: 1 red eye: 1 heavy wing veins: 1 thin wing veins

E) B) and D)
F) All of the above

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In Morgan's experiments, the white eye allele in Drosophila was shown to be


A) located on the X chromosome.
B) located on the Y chromosome.
C) dominant.
D) located on an autosome.

E) All of the above
F) None of the above

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Nondisjunction of a single pair of autosomes can lead to all of the following except


A) aneuploidy.
B) monosomy.
C) trisomy.
D) euploidy.

E) A) and C)
F) All of the above

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Humans who have lost one copy of an autosome are called


A) haploid.
B) trisomic.
C) bisomic.
D) monosomic.

E) B) and C)
F) All of the above

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Hemophilia is caused by a


A) recessive allele on the X chromosome.
B) dominant allele on the X chromosome.
C) codominant allele on the X chromosome.
D) recessive allele on an autosome.

E) A) and C)
F) None of the above

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In sickle cell anemia, the defective hemoglobin differs from the normal hemoglobin by


A) the color of the pigment.
B) the size of the molecule.
C) a single amino acid substitution.
D) the total number of amino acids.

E) A) and B)
F) C) and D)

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Why can't you use mitochondrial DNA to distinguish between these two suspects?


A) The sequence of mitochondrial DNA has not yet been determined.
B) The brothers share the same mitochondrial DNA.
C) There are no molecular techniques available that allow one to analyze mitochondrial DNA.
D) Because mitochondrial DNA is inherited in a paternal pattern.

E) A) and D)
F) All of the above

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A genetic _____ indicates the distances between gene loci measured in terms of the frequency of recombination.


A) map
B) profile
C) pedigree
D) clone

E) C) and D)
F) A) and D)

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A human female with only one X chromosome is said to have a condition called


A) X chromosome inactivation.
B) Angelman syndrome.
C) Turner syndrome.
D) Klinefelter syndrome.

E) B) and C)
F) A) and D)

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How many Barr bodies does a normal human female contain in each diploid cell?


A) 0
B) 1
C) 2
D) 3

E) All of the above
F) B) and C)

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B

In humans, if an XY individual had a deletion of the SYR gene, that person would


A) develop as a female.
B) have both male and female characteristics.
C) have ambiguous genitalia.
D) develop as a male.

E) B) and C)
F) A) and B)

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The number of allele pairs that assort independently in an organism is generally much higher than the number of chromosome pairs.This phenomenon is due to


A) independent assortment.
B) segregation.
C) crossing over.
D) sex-linkage.

E) A) and D)
F) B) and C)

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C

What is the relationship between recombination frequency and the actual physical distance on a chromosome?


A) As physical distance increases, the recombination frequency increases in a linear fashion.
B) As physical distance increases, the recombination frequency decreases in a linear fashion.
C) As physical distance increases, the recombination frequency first increases in a linear fashion, but gradually levels off to a frequency of 0.5.
D) As physical distance increases, the recombination frequency first increases, but then decreases.

E) C) and D)
F) None of the above

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Which statement about calico cats is false?


A) Calico cats can be male or female.
B) The different colored fur is due to the inactivation of one X chromosome.
C) The variation in coat color is an example of an epistatic interaction.
D) Calico cats are genetic mosaics.

E) B) and C)
F) C) and D)

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If you needed to determine the order of genes on a chromosome, you should perform


A) a test cross.
B) a two-point cross.
C) a three-point cross.
D) a SNP test.

E) None of the above
F) A) and B)

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Sickle cell anemia is caused by a defect in the


A) oxygen-carrying pigment hemoglobin.
B) ability of the blood to clot.
C) ability of red blood cells to fight infection.
D) chloride ion transport protein.

E) A) and D)
F) B) and D)

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Occasionally, chromosomes fail to separate during meiosis, leading to daughter cells that have an abnormal number of chromosomes.This phenomenon is called


A) epistasis.
B) nondisjunction.
C) crossing over.
D) pleiotropy.

E) None of the above
F) A) and D)

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B

In humans, if non-disjunction led to an individual with a genotype of XO, that person would


A) be female because each cell lacks a Y chromosome.
B) be male because each cell has only one X chromosome.
C) display both male and female characteristics.
D) not survive.

E) A) and B)
F) C) and D)

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Genetic exchange between 2 homologous chromosomes is called


A) synapsis.
B) pleiotropy.
C) crossing over.
D) allelic exchange.

E) A) and C)
F) All of the above

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_______________ is a human hereditary disease that is caused by a dominant allele but does not show up in affected individuals until they are in middle age.


A) Cystic fibrosis
B) Sickle cell anemia
C) Tay-Sachs disease
D) Huntington's disease

E) A) and B)
F) A) and C)

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