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Hemophelia is an X-linked recessive disorder.A mother without the allele and a father with the allele have a daughter.The daughter then marries a man with hemophilia.What is the genotype of the daughter? What is the probability that the daughter's children will develop the disease?

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A Punnett square will show tha...

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Women do not express X-linked recessive characters.

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Aneuploid human embryos are least likely to survive except those involving:


A) chromosome 1, 2, 3, X, Y.
B) chromosome 1, 2, 3, 4, 5.
C) chromosome 13, 18, 21, X, Y.
D) chromosome 6, 7, 8, 9, 10.
E) chromosome 11, 12, 14, 15.

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Match the following.

Premises
This produces cri-du-chat syndrome.
This has been involved in producing gene families and has been vital to evolution.
This event may occur during meiosis I or meiosis II.
Only 1 percent of human embryos with this condition survive.
Non-homologous chromosomes have exchanged parts.
Responses
aneuploidy
translocation
nondisjunction
deletion
duplication

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This produces cri-du-chat syndrome.
This has been involved in producing gene families and has been vital to evolution.
This event may occur during meiosis I or meiosis II.
Only 1 percent of human embryos with this condition survive.
Non-homologous chromosomes have exchanged parts.

What is one difference between polyploidy and aneuploidy?


A) Polyploidy is extra sets of chromosomes; aneuploidy occurs when there are either more or fewer chromosomes than normally exist in its species full set.
B) Humans can be viable as polyploids but not as aneuploids.
C) Polyploidy is extra sex chromosomes; aneuploidy is extra autosomes.
D) Polyploidy is one extra chromosome; aneuploidy is one missing chromosome.
E) Polyploidy causes diseases and disorders in humans; aneuploidy does not.

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Red-green color blindness is an X-linked recessive trait in humans.A color-blind woman and a man with normal vision have a son.What is the probability that the son is color blind?


A) 100 percent
B) 75 percent
C) 50 percent
D) 25 percent
E) 0 percent

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A woman who does not carry the color-blindness allele has children with a man who is color blind.What proportion of their children will be color blind?


A) all
B) 1/4
C) 1/2
D) 3/4
E) none

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Genes not found on the sex chromosomes will be found on:


A) X chromosomes.
B) Y chromosomes.
C) autosomes.
D) centrosomes.

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Which of the following is an autosomal recessive disorder?


A) hemophilia
B) Huntington disease
C) Down syndrome
D) sickle-cell anemia
E) Turner syndrome

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If a daughter expresses an X-linked recessive gene,she probably inherited the trait from:


A) her mother.
B) her father.
C) both parents.
D) neither parent.
E) her grandmother.

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Explain what causes aneuploidy.

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Nondisjunction is failure of homologous ...

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The human genome has how many pairs of autosomal chromosomes?


A) 46 pairs
B) 44 pairs
C) 23 pairs
D) 22 pairs
E) 24 pairs

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Hemophilia,Duchenne muscular dystrophy,and color blindness are examples of ________ disorders.

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What single attribute determines that a human fetus is male?


A) the absence of a second X chromosome
B) the absence of a Y chromosome
C) the presence of a Y chromosome
D) the presence of two X chromosomes

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What do hemophilia,Duchenne muscular dystrophy,and red-green color blindness have in common?


A) They are X-linked.
B) They are more common in females than in males.
C) They are caused by inheritance of an extra sex chromosome.
D) They are caused by inheritance of an extra autosome.
E) The gene that causes them is on the Y chromosome.

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A karyotype reveals that a woman is carrying a fetus that has 47 chromosomes.The test reveals that the genotype of the fetus is XXY.Which of the following statements is correct?


A) The fetus has Down syndrome, and most likely a nondisjunction event occurred in the mother during egg formation.
B) The fetus has Turner syndrome, and most likely a nondisjunction event occurred in the mother during egg formation.
C) The fetus has Klinefelter syndrome.
D) The fetus has an autosomal disorder.

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If a disease is caused by a dominant allele,it means that a person with the disease:


A) will always pass it on to all their children.
B) will pass it on to one-fourth of their children.
C) must be homozygous dominant for the allele.
D) must be heterozygous for the allele.
E) could be either homozygous or heterozygous for the allele.

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Duchenne muscular dystrophy is a recessive disorder resulting in a wasting away of the muscles.How would you design a study to determine if the disorder is X-linked or autosomal? How would you be able to determine if it is X-linked or autosomal?

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The study would analyze the inheritance ...

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Polyploidy is better tolerated in plants than in animals.

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The state of having more than two sets of chromosomes is called:


A) autosomal.
B) dominant.
C) polyploidy.
D) aneuploidy.
E) nondisjunction.

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