A) A mother and father both have type O blood, and their son is born with type B blood.
B) Two children in the same family both have sickle cell disease, but one child has more severe symptoms than the other.
C) Monozygotic twins separated at birth and raised in two different countries are of different heights (3 inches) and different weights (25 pounds) .
D) A woman who has a gene mutation for diabetes mellitus type 2 delays the onset of the disease by exercising and maintaining a normal weight.
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Multiple Choice
A) Decreased penetrance of a dominant trait
B) Variable expressivity of a recessive trait
C) Inactivation of both parents' X chromosomes
D) Failure of one parent's blood-type gene alleles to segregate
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Multiple Choice
A) Hypertension
B) Peptic ulcer disease
C) Congenital heart disease
D) Schizophrenic behavior
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Multiple Choice
A) The child with the disorder is male, and the overall incidence of the disorder is twice as high in males than females.
B) Both the mother and the father are heavily exposed to a variety of chemicals in their workplaces.
C) The father has a nephew with a mild form of the same disorder.
D) The mother has a brother who also has the same disorder.
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Multiple Choice
A) 100%
B) 75%
C) 50%
D) 25%
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Multiple Choice
A) Yes, because the disorder is autosomal dominant, and if both parents are heterozygous, the child could inherit two normal stature gene alleles.
B) Yes, if the parent who is homozygous for the gene mutation demonstrates variable expressivity of the health problem.
C) No, because the disorder is autosomal recessive, and the child can only inherit two mutated gene alleles for the health problem.
D) No, because homozygosity for this health problem is lethal.
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Multiple Choice
A) The same gene may have more than one chromosome locus.
B) The protein coded for by the single gene is an important component of more than one tissue.
C) The silencing of a gene allele inherited from one parent is expressed differently depending on which parent contributed the silenced allele.
D) The same disorder may have an autosomal-dominant inheritance pattern, an autosomal-recessive inheritance pattern, and an X-linked-recessive inheritance pattern.
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Multiple Choice
A) The risk for a person who is homozygous for the trait to transmit the trait to his or her children is 100% with each pregnancy.
B) The trait often remains unexpressed within a kindred for many generations until a change in environment promotes its expression.
C) Males in a kindred are more likely to express the trait when the mother has the trait, and females in a kindred are more likely to express the trait when the father has the trait.
D) Females in a kindred are more likely to express the trait when the mother has the trait, and males in a kindred are more likely to express the trait when the father has the trait.
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Multiple Choice
A) Autosomal dominant
B) Autosomal recessive
C) X-linked dominant
D) Codominant
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Multiple Choice
A) P1
B) P2
C) F1
D) F2
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Multiple Choice
A) Two hearing-impaired parents produce a child who has normal hearing.
B) A 40-year-old man whose father developed type 2 diabetes mellitus at age 50 is diagnosed with the disorder.
C) The three children of a mother who has an intelligence quotient (IQ) of 170 all have IQs in the 110 to 120 range.
D) A child whose biologic parents are thin is adopted by a family whose members are obese and eventually becomes overweight.
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Multiple Choice
A) Widow's peak
B) Diabetes mellitus type 2
C) Polycystic kidney disease
D) Taste sensitivity to phenylthiocarbamate (PTC)
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Multiple Choice
A) The threshold required for disease expression increases as the population ages.
B) The number of affected individuals within the population has decreased.
C) The population examined for the potential problem is getting larger.
D) The threshold required for disease expression is lower.
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Multiple Choice
A) A person with low expressivity of the trait has a higher probability of having a child who does not express the trait at all.
B) A person with high expressivity of the trait has a greater risk of having a child who expresses the trait to an even greater degree.
C) The degree of expressivity of a given autosomal-dominant trait with known variability cannot be predicted by analyzing parental expression.
D) The degree of expressivity of a given autosomal-dominant trait with known variability is greater when the transmitting parent is the same sex as the child.
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Multiple Choice
A) Short tongue dominant; long tongue recessive
B) Short tongue recessive; long tongue dominant
C) Short tongue dominant; long tongue dominant
D) Short tongue dominant; long tongue X-linked recessive
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Multiple Choice
A) Dizygotic twins share fewer allele sequences in common than monozygotic twins.
B) It is possible for dizygotic twins to have different fathers, and monozygotic twins always have the same father.
C) Gene expression in monozygotic twins is less influenced by environmental factors than that of dizygotic twins.
D) Because of their identical appearance, monozygotic twins are more likely to be raised together and share a common environment than are dizygotic twins.
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Multiple Choice
A) Syndactyly
B) Phenylketonuria
C) Long QT syndrome
D) Retinitis pigmentosa
Correct Answer
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Multiple Choice
A) A mutation in a single gene results in the expression of problems in a variety of tissues and organs.
B) The susceptibility to a problem is an inherited trait, but development of the problem is related to environmental conditions.
C) A mutated gene is inherited, but the results of expression of that gene are not evident until middle or late adulthood.
D) Several genes are responsible for the mechanism of hearing, and a mutation in any one of them results in hearing impairment.
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Multiple Choice
A) Carriers for the trait may express it but do not necessarily express the trait.
B) Unaffected family members do not transmit the trait to their children.
C) Genotypes of individuals expressing the trait must be homozygous.
D) The trait appears only among male offspring of female carriers.
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Multiple Choice
A) All sons will be unaffected; all daughters will be carriers.
B) All sons will be carriers; all daughters will be affected.
C) All sons have a 50% risk of the disorder; daughters will all either be affected or carriers.
D) All sons will be carriers; daughters have a 50% chance of being a carrier and a 50% chance of being unaffected.
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