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5 Written Questions

5 Matching Questions

  1. Trait
  2. Mutation
  3. Complication
  4. Protein
  5. Chromosome
  1. a A secondary disease or condition that develops in the course of a primary disease or condition and arises either as a result of it or from independent causes
  2. b An inherited characteristic
  3. c A 3-D biological polymer constructed from a set of 20 different monomers called amino acids
  4. d A rare change in the genetic material, ultimately creating genetic diversity
  5. e Any of the usually linear bodies in the cell nucleus that contain the genetic material

5 Multiple Choice Questions

  1. A condition that appears only in individuals who have received two copies of a mutant gene, one copy from each parent
  2. Deformed red blood cells that can lead to numerous symptoms and caused by a genetic mutation in the hemoglobin protein
  3. A discrete unit of hereditary information
  4. Capable of being transmitted from person to person, animal to animal, animal to human, or human to animal by contact
  5. An iron-containing protein in red blood cells that reversibly binds oxygen

5 True/False Questions

  1. AnemiaA condition in which the blood is deficient in red blood cells, in hemoglobin, or in total volume.

          

  2. AutosomeA chromosome that is not directly involved in determining sex, as opposed to sex chromosome

          

  3. SymptomSubjective evidence of disease or physical disturbance observed by the patient

          

  4. KaryotypeA 3-D biological polymer constructed from a set of 20 different monomers called amino acids

          

  5. Sex ChromosomeAny of the usually linear bodies in the cell nucleus that contain the genetic material

          

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