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2. The inability of the dominant allele to make up for the presence of the recessive allele is associated with _____. A. codominance B. epistasis C. incomplete dominance D. pleiotropy. ___.

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  1. 2. The inability of the dominant allele to make up for the presence of the recessive allele is associated with _____. A. codominance B. epistasis C. incomplete dominance D. pleiotropy ___

  2. 4. If the allele for red petals is not completely dominant to the allele for white petals, when a true-breeding plant with red petalsis crossed with a true breeding plant with white petals, the offspring will ____. A. all have red petals B. all have pink petals C. all have white petals D. all have red and white petals ___

  3. 5. When the plants with pink petals (R1R2) are allowed to self-pollinate, the phenotypic ratio of the offspring will be _____. A. 3:1 B. 1:1:1:1 C. 1:2:1 D. 9:3:3:1 ___

  4. 8. The appearance of both A and B types of glycoproteins on the red blood cells of the people with AB blood type is anexample of _______. A. codominance B. polygenic inheritance C. epistasis D. incomplete dominance ___

  5. 9. In _____, genes at two different loci interact to control a single trait. A. codominance B. pleiotropy C. polygenic inheritance D. epistasis ___

  6. 10. Albinism is the result of _____. A. epistasis B. pleiotropy C. codominance D. incomplete dominance ___

  7. 11. If sweet peas are _____ in either gene for pigmentation, a lack of color results. A. homozygous dominant B. heterozygous C. homozygous recessive ___

  8. 12. An absence of color occurs when _____. A. a gene is absent B. an enzyme in a metabolic pathway is missing C. at least one dominant allele is present ___

  9. 13. Polygenic inheritance occurs when one trait is governed by many genes occupying different loci on ______. A. the same homologous pair of chromosomes B. different homologous pairs of chromosomes C. either A or B D. neither A or B ___

  10. 14. More than two possible phenotypes for a particular trait can be attributed to inheritance by _____. A. simple dominance B. multiple alleles C. epistasis D. pleiotropy ___

  11. 15. Blood type in humans is controlled by _____ allele(s). A. one B. two C. three D. four ___

  12. 17. When there is a range of phenotypes, the inheritance is _____. A. polygenic B. codominant C. incompletely dominant D. pleiotropic ___

  13. 19. When individuals make an abnormal form of the extracellular matrix protein, fibrillin, which affects many other traits, theinheritance is the result of ______. A. codominance B. multiple alleles C. simple dominance D. pleiotropy ___

  14. 20. More phenotypes than expected may result from polygenic inheritance because of _____. A. multiple alleles B. codominance C. environmental effects D. pleiotropy ___

  15. 22. Height in humans is affected by _____. A. polygenic inheritance B. environmental effects such as nutrition C. both A and B ___

  16. 23. Environmental conditions can influence _____. A. the skin color of humans B. the fur color of rabbits C. the appearance of a water buttercup D. all of the above ___

  17. 27. Which of the following supports the chromosomal theory of inheritance? A. both chromosomes and alleles are paired in diploid cells B. homologous chromosomes and alleles separate during meiosis C. fertilization restores both the diploid chromosome number and allele pairs in the zygote. D. all of the above ___

  18. 28. Who determines the sex of the child? A. the male B. the female ___

  19. 30. The sex chromosomes of a human female are _____. A. XX B. XY C. YY ___

  20. 33. Male and female Drosophila flies have _____. A. the same number of chromosomes as humans B. one pair of sex chromosomes C. the same number of sex chromosomes as humans D. both B and C ___

  21. 34. The allele for Drosophila eye color ____. A. is on the Y chromosome B. is on the X chromosome C. is on one of its autosomes ___

  22. 37. Which of the following best describes a Drosophila with the genotype XRXr assuming XR = red eyes and Xr = white eyes? A. female with red eyes B. female that is a carrier C. male with white eyes D. both A and B ___

  23. 38. Assuming XR = red eyes and Xr = white eye, what is the phenotype of an individual with the genotype XrY? A. male with red eyes B. male with white eyes C. female with red eyes D. female with white eyes ___

  24. 39. An individual with the genotype XrY will produce which of the following gametes? A. XR B. Xr C. Y D. both B and C ___

  25. 43. If XB = normal vision and Xb = color blindness, what are the chances a color blind female will have color blind sons if shehas children with a man with normal vision? A. 100% B. 50% C. 25% D. none ___

  26. 44. What are the chances of a female, homozygous for normal vision, and a color blind male having color blind daughters? A. 100% B. 50% C. 25% D. none ___

  27. 45. Carriers can also be described as _____. A. homozygous recessive B. homozygous dominant C. heterozygous ___

  28. 47. There is a direct relationship between the frequency of crossing-over and the percentage of recombinant __________. A. gametes B. phenotypes C. genotypes ___

  29. 48. The chromosomes can be mapped by determining the frequency of recombinant _____ that occurs due to the process ofcrossing over. A. gametes B. phenotypes C. genotypes ___

  30. 49. Drosophila chromosome II carries the gene for _____. A. antennae type B. wing type C. leg length D. all of the above ___

  31. 50. If crossing over occurs between two linked alleles of interest, a dihybrid produces _____ type(s) of gamete(s). A. one B. two C. three D. four ___

  32. 51. When chromosomes are mapped by examining recombinant phenotypes, it is assumed that 1% of crossing over equals_____ map unit(s). A. one B. two C. five D. ten ___

  33. 52. When individuals heterozygous for two traits that have linked alleles are crossed the expected phenotypic ratio of theoffspring is _____. A. 1:1:1:1 B. 1:1 C. 3:1 D. 9:3:3:1 ___

  34. 53. When a cross involving mutant genes b and e is done 3% recombinants are observed. When a cross involving mutantgenes t and e is done 22% recombinants are observed. When a cross involving mutant genes b and t is done 19%recombinants are observed. What is the correct order of the genes on the chromosome? A. t, b, e B. b, t, e C. t, e, b ___

  35. 55. It is estimated that __________ of all flowering plants are polyploids. A. 21% B. 47% C. 68% D. 92% ___

  36. 56. Triploids have _____ of each kind of chromosome. A. one B. two C. three D. four ___

  37. 57. Nondisjunction can occur during meiosis I if _____. A. members of a homologous pair fail to separate B. the daughter chromosomes fail to separate and instead go into the same daughter cell C. both A and B ___

  38. 59. When an individual has only one of a particular type of chromosome it's described as _____. A. monosomy B. disomy C. trisomy D. tetrasomy ___

  39. 62. Down syndrome is a _____. A. monosomy B. disomy C. trisomy D. tetrasomy ___

  40. 63. In humans, Turner syndrome _____. A. is a monosomy B. involves the sex chromosomes C. results in a female D. all of the above ___

  41. 64. Nondisjunction can occur during _____. A. anaphase I B. anaphase II C. both A and B ___

  42. 65. A trisomy occurs when an individual has three of _____. A. a particular type of chromosome B. each kind of chromosome C. both A and B ___

  43. 67. Polyploidy generally results from _____. A. mutation B. hybridization C. nondisjunction ___

  44. 68. Which of the following is a polyploid? A. wheat B. watermelons C. cotton D. all of the above ___

  45. 70. A(n) _____ is the movement of a segment of a chromosome from one chromosome to another nonhomologouschromosome. A. inversion B. translocation C. deletion D. duplication ___

  46. 71. When a broken segment from one chromosome attaches to its homologue a(n) _____ occurs. A. duplication B. deletion C. inversion D. both A and B ___

  47. 72. Which of the following may result in abnormal gametes and offspring? A. inversion B. translocation C. deletion D. all of the above ___

  48. 75. Down syndrome that tends to run in the family of either the mother or father is the result of _____. A. deletion B. inversion C. duplication D. translocation ___

  49. 76. Cri du chat syndrome is the result of a(n) _____. A. inversion B. translocation C. deletion D. duplication ___

  50. 78. Chromosomes may be broken by _____. A. viruses B. radiation C. certain organic chemicals D. all of the above ___

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