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Among the disorders caused by changes in chromosome structure are all but one of those listed below; that one is


A) Fragile X syndrome
B) Klinefelter syndrome
C) Williams syndrome
D) Cri du chat syndrome
E) All of these are caused by a change in chromosome structure

F) A) and E)
G) A) and D)

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Considering that males can have Klinefelter (XXY) syndrome,XYY,and normal XY chromosomal combinations,and females can have Turner (XO) syndrome,poly-X (XXX,XXXX) ,and normal XX combinations,it is obvious that


A) maleness results from the presence of only one X chromosome.
B) maleness results from the absence of two or more X chromosomes.
C) maleness results from the minimal presence of one Y chromosome.
D) femaleness results from the presence of two or more X chromosomes.
E) sex determination is a delicate balance between X and Y chromosomes.

F) A) and E)
G) A) and B)

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A karyotype will NOT reveal which of the following genetic diseases?


A) Turner syndrome
B) Klinefelter syndrome
C) Down syndrome
D) cri du chat syndrome
E) hemophilia

F) A) and D)
G) A) and C)

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Karyotyping can be used to diagnose which of the following genetic disorders?


A) Down syndrome
B) phenylketonuria
C) neurofibromatosis
D) cystic fibrosis
E) hemophilia

F) A) and E)
G) D) and E)

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An XXX female would most likely result from nondisjunction in


A) the mother during egg formation.
B) the father during sperm formation
C) in both the mother and father during gamete formation.
D) the fertilized egg.
E) neither the mother nor the father.

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

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All of the genes on a single chromosome are


A) A locus
B) Homologous
C) A linkage map
D) A linkage group
E) An allele

F) B) and C)
G) B) and D)

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If a person inherits two X chromosomes,this individual will be


A) female.
B) male.
C) colorblind.
D) sterile.
E) a poly-X female.

F) B) and D)
G) A) and B)

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A person who has an extra copy of a chromosome is said to have


A) monosomy.
B) bisomy.
C) trisomy.
D) nondisjunction.
E) duplication.

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

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Which genetic trait is NOT associated with the chromosome involved in Down syndrome?


A) increased incidence of leukemia
B) cataracts
C) mental retardation
D) accelerated aging
E) cystic fibrosis

F) A) and E)
G) D) and E)

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If a woman is a carrier for the color blind recessive allele and her husband is normal,what are their chances that a son will be color blind?


A) None since the father is normal.
B) 50%, since the mother is only a carrier.
C) 100% because the mother has the gene.
D) 25% because the mother is a hybrid.
E) None since the son will also be just a carrier.

F) C) and D)
G) A) and B)

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Which of the following is NOT true about a karyotype?


A) Homologous chromosomes are arranged in pairs.
B) Sex chromosomes are identified separately from autosomes.
C) All chromosome pairs are numbered differently for males and females.
D) Chromosome pairs are assorted by both size and shape.
E) Banding patterns are used in pairing chromosomes.

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

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A colorblind (recessive trait) woman will pass the allele to


A) her sons only.
B) all her children.
C) her daughters only.
D) none of her children.
E) her husband.

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

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An individual who has an XXY combination of sex chromosomes is said to have _____ syndrome.


A) Klinefelter
B) Turner
C) Down
D) fragile X
E) cri du chat

F) A) and B)
G) C) and D)

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Describe a genetic disorder associated with a deletion in chromosomal number.

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Williams syndrome occurs when chromosome...

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A female with two Barr bodies in her cells would have what combination of sex chromosomes?


A) XXY
B) XXXY
C) XXX
D) XX
E) XYY

F) A) and E)
G) B) and E)

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Genes on the ___ chromosome determine if the sex of a child will be male or female.


A) X
B) Y
C) 21st
D) 5th
E) 19th

F) B) and C)
G) None of the above

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Which refers to the addition of a repeat segment of a chromosome?


A) inversion
B) translocation
C) deletion
D) duplication
E) monosomy

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

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List the four X-linked recessive disorders.

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1.Color blindness
2....

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