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In a dihybrid cross,in which both parents are heterozygous for both traits,what is the probability that the offspring will exhibit both of the dominant phenotypes?


A) 1/16.
B) 3/16.
C) 6/16.
D) 9/16.
E) 1.

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Explain the problems associated with the genetic disorder Tay-Sachs. A. This lysosome is responsible for clearing out the fatty acids that build up in the cells of the brain. The buildup begins to interfere with proper brain development and growth. This leads to malfunctions in vision, movement, hearing, and overall mental development. The impairment leads to blindness, seizures, paralysis, and death.

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Affected children w...

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If you want to know the probability that tossing two coins will result in a particular outcome (two heads,for example) ,you use the


A) product rule.
B) sum rule.
C) punnett rule.
D) Bergman's rule.
E) genetics rule.

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In a pedigree,an affected male would be designated by


A) an open circle.
B) a shaded circle.
C) an open square.
D) a shaded square.
E) a square with a line through it.

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Which of the following is an example of a homozygous recessive genotype?


A) aa
B) Aa
C) short
D) AA
E) ab

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Which of the following is not a characteristic of an X-linked recessive disorder pedigree?


A) An affected son can have normal parents.
B) If a female has the trait, her father must also have it.
C) The characteristic often skips a generation.
D) More females than males are affected.
E) If a woman has the characteristic, all of her sons will have it.

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What is the genotype of a person with type O blood?


A) IAIA
B) IAIB
C) IAi
D) IBi
E) ii

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Which of the following represents a cross to determine if an individual is homozygous dominant or heterozygous?


A) Aa x aa
B) AA x AA
C) aa x aa
D) Aa x AA
E) Aa x Aa

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Which of the following would not be a common/conventional way to list someone's genotype?


A) BB
B) Bb
C) AB
D) bb
E) AA

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Even though sickle-cell disease is inherited as an autosomal recessive disorder,the heterozygote can express some variation of the recessive phenotype.

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How are Fragile X syndrome and Huntington disease similar?


A) Both exhibit a late onset in life.
B) Both are trinucleotide-repeat expansion disorders.
C) Both affect the muscles and lead to eventual paralysis.
D) Both cause autism.
E) Both are found only in males.

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B

Which of the following is not a characteristic of an autosomal dominant disorder pedigree?


A) Affected children will usually have unaffected parents.
B) Heterozygotes are affected.
C) Two affected parents can produce an unaffected child.
D) Both males and females are affected with equal frequency.
E) Two unaffected parents will not have affected children.

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The definition of a multifactorial trait is one in which more than one set of alleles is involved,in which the environment plays no role.

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Which of the following disorders is caused by a defect in the production of an elastic connective tissue protein called fibrillin?


A) cystic fibrosis
B) Tay-Sachs disease
C) Marfan syndrome
D) Huntington disease
E) sickle-cell disease

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C

If a person with type B blood marries a person with type A blood,what phenotypes can their children be?


A) all type A
B) all type B
C) types A and O
D) types B and O
E) types A, B, O, and AB

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There is a single gene that controls the ability to taste PTC paper.The ability to taste is dominant to the inability to taste.If you can taste the paper,it is very bitter.Which of the following genotypes can taste the paper?


A) only PP
B) both PP and Pp
C) both PP and pp
D) only Pp
E) only pp

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Which of the following traits would not be considered multifactorial?


A) alcoholism
B) suicide risk
C) cleft lip/palate
D) diabetes
E) ABO blood type

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Which of the following is not an autosomal recessive disorder?


A) Marfan syndrome
B) Tay-Sachs disease
C) cystic fibrosis
D) sickle-cell disease
E) All are autosomal recessive disorders.

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In a cross of a homozygous dominant parent and a homozygous recessive parent,what is the ratio of offspring that will exhibit the recessive phenotype?


A) 0.
B) 1/4.
C) 1/2.
D) 3/4.
E) 1.

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A

How is familial hypercholesterolemia inherited?


A) autosomal recessive
B) autosomal dominant
C) incompletely dominant
D) codominant
E) sex-linked dominant

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