CH 4 Genes and Genetic Diseases

  1. Inserting bone marrow cells into an individual who produces abnormal erythrocytes is an
    example of what type of therapy?



    A.
  2. DNA replication requires the enzyme DNA polymerase to:
    a. Travel along the single DNA strand, adding the correct nucleotide to the new
    strand
    b. Move along the double strand of DNA to unwind the nucleotides of the double
    helix
    c. Hold the double strand apart while the correct nucleotides are added to the strand
    d. Transport the double strand of DNA from the nucleus to the cytoplasm for protein
    formation
    a.
  3. Transcription is best defined as a process by which:



    C.
  4. The purpose of a staining technique of chromosomes such as Giemsa is to:



    A.
  5. An amniocentesis indicates a neural tube defect when an increase in which protein is
    evident?



    D.
  6. The most clinically useful technique for prenatal diagnosis of chromosomal abnormalities
    at 3 months’ (12 weeks’) gestation is:



    D.
  7. The term for an error in which homologous chromosomes fail to separate during meiosis
    or mitosis is:



    D.
  8. Which clinical manifestations would be expected for a child who has complete trisomy of
    the twenty-first chromosome?



    D.
  9. What is the most common cause of Down syndrome?



    A.
  10. What syndrome, characterized by an absent homologous X chromosome with only a single
    X chromosome, exhibits features that include a short stature, widely spaced nipples, and
    webbed neck?



    B.
  11. A person with 47, XXY karyotype has the genetic disorder resulting in which syndrome?



    D.
  12. What is the chromosomal variation that causes Klinefelter syndrome?



    D.
  13. What is the second most commonly recognized genetic cause of mental retardation?



    B.
  14. Males are more often affected by which type of genetic disease?



    B.
  15. The presence of a zygote having one chromosome with the normal complement of genes
    and one with a missing gene is characteristic of which genetic disorder?



    A.
  16. A child with which genetic disorder has a characteristic cry?



    B. (cry of the cat)
  17. The key to accurate DNA replication depends on which complementary base pairs? (Select
    all that apply.)
    a. Adenine with thymine
    b. Adenine with guanine
    c. Guanine with cytosine
    d. Cytosine with thymine
    e. Guanine with thymine
    a, c
  18. Examples of prenatal diagnostic studies include: (Select all that apply.)
    a. Chorionic villus sampling (CVS)
    b. Amniocentesis
    c. Carrier screening
    d. Preimplantation genetic diagnosis (PGD)
    e. Drug-sensitivity testing
    a, b, d.
  19. Cystic fibrosis
    autosomal recessive
  20. A display of chromosomes ordered according to length and centromere location is called a _______________.
    karyotype
  21. A _______________ mutation of DNA involves addition or deletion of a number of base pairs that is not a multiple of three and thus alters all of the codons downstream from the site of insertion or deletion.
    frameshift
  22. Interchanging of genetic material between nonhomologous chromosomes is called _______________
    translocation
  23. Write the letters here in the correct order of the steps:
    A. Translation
    B. Transcription
    C. mRNA leaves the nucleus
    D. RNA polymerase binds to DNA promoter region
    E. mRNA is spliced to remove noncoding sections
    d, b, e, c, a
Author
BodeS
ID
362390
Card Set
CH 4 Genes and Genetic Diseases
Description
Genes and Genetic Diseases
Updated