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In Down syndrome,


A) as the age of the mother increases, the chance of the defect occurring in the unborn children increases.
B) the age of the father usually has an equal influence on the defect.
C) most embryos abort before complete term.
D) a person with the defect cannot have a normal child.
E) 80% of trisomic 21 babies are born to women over the age of 40.

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One of the major symptoms of Marfan syndrome is


A) hypertension.
B) rupture of the aorta.
C) retardation.
D) short stature.
E) abnormally short arms and legs.

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Tay-Sachs disease is most common among


A) Blacks.
B) Hispanics.
C) Asians.
D) Jewish people of Eastern European descent.
E) Native Americans.

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Tay-Sachs disease


A) is controlled by a simple recessive gene.
B) is a sex-linked disease more common in males.
C) occurs only in those individuals that receive two copies of a defective recessive gene.
D) is the result of the failure of chromosomes to separate so that an individual receives three instead of two chromosomes.
E) depends on which parent passes the gene to the child.

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The condition occurring when an organism has a 2 n + 1 chromosome composition is known as


A) monosomy.
B) trisomy.
C) diploid.
D) haploid.
E) both trisomy and haploid.

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Selecting the Exception Four of the five answers listed below are caused by recessive genes. Select the exception.


A) Huntington's disorder
B) phenylketonuria
C) color blindness
D) hemophilia
E) albinism

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Aneuploidy would describe all of the following except


A) Turner syndrome.
B) Klinefelter syndrome.
C) translocation.
D) XYY.
E) Down syndrome.

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Which of the following designates a normal human female?


A) XXY
B) XY
C) XX
D) XYY
E) XO

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Genes are


A) located on chromosomes.
B) inherited in the same way as chromosomes.
C) arranged in linear sequence on chromosomes.
D) may be exchanged between homologous chromosomes.
E) all of these.

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Which of the following statements is false?


A) The SRY gene is absent in females.
B) The SRY gene apparently is the gene that controls the development of male sexuality.
C) The development of maleness is by default because males lack two X chromosomes.
D) Genes on an X chromosome are called X-linked.
E) There is no difference in external genitalia of males or females until four weeks after conception when the genes determining sex begin to be expressed.

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Which of the following designates a normal human male?


A) YY
B) XX
C) XY
D) XO
E) XYY

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In a pedigree chart, a male showing the specific trait being studied is indicated by a


A) darkened square.
B) clear square.
C) darkened diamond.
D) clear triangle.
E) darkened circle.

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If the gene for yellow body color ( y ) is an X-linked recessive and its dominant counterpart ( y +) produces wild body colors, give the phenotypes expected and their frequencies for the following four crosses: (a) yellow female x wild male (b) wild carrier female x wild male (c) wild carrier female x yellow male (d) homozygous wild female x yellow male

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(a) yellow male, wild female
(b) 1/4 w...

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If an embryo doesn't have an exact multiple of the normal haploid number of 23 chromosomes, the condition is known as


A) aneuploidy.
B) diploidy.
C) ahaploidy.
D) multiploidy.
E) synploidy.

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Concerning the sex chromosomes, which of the following is correct?


A) The Y chromosome carries a greater number of nonsexual traits.
B) X and Y are different in size but carry nearly equal numbers of genes.
C) The X chromosome carries more genes for nonsexual traits.
D) The X chromosome carries only gender-related genes.
E) The X chromosome carries the SRY gene.

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A female who is heterozygous for hemophilia will


A) exhibit the condition throughout her life.
B) suffer from bleeding when severely stressed.
C) show no signs of the disease at all.
D) pass the gene on to all of her children.
E) pass the gene on to only her sons.

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A genetically directed deviation from the average is called


A) an abnormality.
B) a disorder.
C) a syndrome.
D) a carrier.
E) a pedigree.

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Karyotype analysis


A) is a means of detecting and reducing mutagenic agents.
B) is a surgical technique that separates chromosomes that have failed to segregate properly during meiosis II.
C) can be used in prenatal diagnosis to detect chromosomal mutations and genetic disorders in embryos.
D) replaces defective alleles with normal ones.
E) is used in DNA analysis for paternity.

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Color blindness is an X-linked recessive gene. Two normal-visioned parents produce a color-blind child. (a) Is this child male or female? (b) What are the genotypes of the parents? (c) What are the chances that their next child will be a color-blind daughter?

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(a) male
(b) Cc x ...

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If a human recessive X-linked characteristic occurred with a 10 percent frequency, what would its frequency be in males and females?

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Males 10 p...

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