Genetics Quiz Questions Flashcards

1
Q

T/F The genetic information needed for protein synthesis is encoded in the DNA contained in the cell nucleus.

A

True

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2
Q

T/F Polygenic inheritance can be predicted utilizing the Mendelian laws of genetic transmission.

A

False- single gene disorders

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3
Q

T/F Messenger RNA carries the instructions for protein synthesis

A

True

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4
Q

T/F The genotype refers to the recognizable traits, physical or biochemical, associated with a specific phenotype.

A

False- The PHENOTYPE refers to the recognizable traits, physical or biochemical, associated with a specific GENOTYPE

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5
Q

T/F The Punnett square can be utilized to describe possible combinations that can occur with transmission of single-gene dominant and recessive traits.

A

True

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6
Q

T/F Ribosomal is the type of RNA that functions to deliver the activated form of amino acids to protein molecules in the ribosomes.

A

False- tRNA

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7
Q

T/F Autosomal recessive disorders are manifested even if only one member of the gene pair is affected.

A

False- Autosomal DOMINANT disorders

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8
Q

T/F A teratogenic agent is an environmental agent that produces abnormalities only during the first 4 weeks of embryonic or fetal development

A

False - 15-50 days

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9
Q

T/F Down syndrome, Turner syndrome and Klinefelter syndrome are all examples of chromosomal disorders that occur from an alteration in chromosome number.

A

True

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10
Q

T/F Sex-linked disorders almost always are associated with the X chromosome and are predominantly recessive.

A

True

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11
Q

Which of the following statements about CF is correct?

  • CF is an autosomal dominant trait
  • CF results from a mutation in the CFTR gene, which normally encodes a chloride ion channel
  • the most common mutation associated with CF is a single nucleotide polymorphism (point mutation) in the CFTR gene
  • Normally individuals with a mutation in the CFTR have a normal sweat test
A
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12
Q

A person with cystic fibrosis may be at risk of bleeding due to:

  • Excessive fat digestion
  • Decreased vitamin K absorption
  • Compromised chloride ion transport
  • Increased secretions throughout the gut
A
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13
Q

A person with CF may have decrased fertility

T/F

A

True

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14
Q

Two parents with the trait for sickle cell disease (so they are heterozygotes) have a child. What is the risk of that child having sickle cell disease?

  • 0%
  • 25%
  • 50%
  • 100%
A
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15
Q

Many of the s/s of SCD (hyperbillirubinema, decreased hematocrit, enlarged liver and spleen) are due to excessive hemolysis experienced by individuals with SCD

A

True

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16
Q

Sickle cell disease is an autosomal recessive disease that is caused by a point mutation in the beta globin gene.

T/F

A

True

17
Q

Risk of Down Syndrome may be associated with which of the following?

  • Advanced maternal age
  • Previous child with down syndrome
  • being a carrier of a genetic translocation for Down syndrome
  • All of the above may occur in a child with Downs
A

All of the above

18
Q

Which of the following complications may be evident in a child with Down Syndrome?

  • Heart Defects
  • Hearing Loss
  • Poor Vision
  • All of the above
A

All of the above

19
Q

Parents of a Down syndrome child are typically genetically normal (have a normal karyotype)

T/F

A

True

20
Q

Hemophilia is an example of which type of inheritance?

A

X-linked recessive

21
Q

If Bob has an inherited form of hemophillia, most likely his father would be:

  • a hemophilliac (affected)
  • a carrier
  • unaffected without an affected allele
  • it is not possible to know about bob’s father with regard to his hemophilla status
A

It is not possible to know

22
Q

Hemophillia may be acquired rather than genetic, a form of the disease that involves development of autoantibodies against clotting factors (Factor VIII)

T/F

A

True