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Preview Chapter 12 Multiple Choice Short Response Extended Response

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1 Preview Chapter 12 Multiple Choice Short Response Extended Response
Standardized Test Prep Preview Multiple Choice Short Response Extended Response

2 Chapter 12 Multiple Choice 1. Which can a chromosomal map show?
Standardized Test Prep Multiple Choice 1. Which can a chromosomal map show? A. the sex of the individual B. the presence of mutant alleles C. the positions of genes on a chromosome D. whether a gene is autosomal or recessive

3 Multiple Choice, continued
Chapter 12 Standardized Test Prep Multiple Choice, continued 1. Which can a chromosomal map show? A. the sex of the individual B. the presence of mutant alleles C. the positions of genes on a chromosome D. whether a gene is autosomal or recessive

4 Multiple Choice, continued
Chapter 12 Standardized Test Prep Multiple Choice, continued 2. Which can result from the deletion of a single nucleotide? F. trisomy G. a translocation H. nondisjunction J. a frameshift mutation

5 Multiple Choice, continued
Chapter 12 Standardized Test Prep Multiple Choice, continued 2. Which can result from the deletion of a single nucleotide? F. trisomy G. a translocation H. nondisjunction J. a frameshift mutation

6 Multiple Choice, continued
Chapter 12 Standardized Test Prep Multiple Choice, continued 3. At the present time amniocentesis cannot reveal which of the following? A. eye color B. genetic disease C. sex of the fetus D. chromosomal abnormalities

7 Multiple Choice, continued
Chapter 12 Standardized Test Prep Multiple Choice, continued 3. At the present time amniocentesis cannot reveal which of the following? A. eye color B. genetic disease C. sex of the fetus D. chromosomal abnormalities

8 Multiple Choice, continued
Chapter 12 Standardized Test Prep Multiple Choice, continued 4. A geneticist working with the fruit fly Drosophila melanogaster discovers a mutant phenotype that appears only in males who are offspring of males of the same phenotype. What does this information suggest about the mutant phenotype? F. The trait is X-linked. G. The trait is Y-linked. H. The trait is autosomal dominant. J. The trait is autosomal recessive.

9 Multiple Choice, continued
Chapter 12 Standardized Test Prep Multiple Choice, continued 4. A geneticist working with the fruit fly Drosophila melanogaster discovers a mutant phenotype that appears only in males who are offspring of males of the same phenotype. What does this information suggest about the mutant phenotype? F. The trait is X-linked. G. The trait is Y-linked. H. The trait is autosomal dominant. J. The trait is autosomal recessive.

10 Multiple Choice, continued
Chapter 12 Standardized Test Prep Multiple Choice, continued The table below shows the genotypes and phenotypes of pattern baldness. Use the table to answer the question that follows. 5. Which statement best explains why men and women express the Bb genotype differently? A. The trait is polygenic. B. The trait has multiple alleles. C. Pattern baldness is a sex-linked trait. D. Pattern baldness is a sex-influenced trait.

11 Multiple Choice, continued
Chapter 12 Standardized Test Prep Multiple Choice, continued The table below shows the genotypes and phenotypes of pattern baldness. Use the table to answer the question that follows. 5. Which statement best explains why men and women express the Bb genotype differently? A. The trait is polygenic. B. The trait has multiple alleles. C. Pattern baldness is a sex-linked trait. D. Pattern baldness is a sex-influenced trait.

12 Multiple Choice, continued
Chapter 12 Standardized Test Prep Multiple Choice, continued 6. translocation : chromosome mutation :: substitution F. gene mutation G. point mutation H. germ-cell mutation J. somatic-cell mutation

13 Multiple Choice, continued
Chapter 12 Standardized Test Prep Multiple Choice, continued 6. translocation : chromosome mutation :: substitution F. gene mutation G. point mutation H. germ-cell mutation J. somatic-cell mutation

14 Multiple Choice, continued
Chapter 12 Standardized Test Prep Multiple Choice, continued The image below is a pedigree showing the inheritance of hemophilia in a family. Use the pedigree to answer the question that follows. 7. Which type of inheritance pattern is associated with hemophilia? A. autosomal recessive B. sex-linked dominant C. sex-linked recessive D. autosomal dominant

15 Multiple Choice, continued
Chapter 12 Standardized Test Prep Multiple Choice, continued The image below is a pedigree showing the inheritance of hemophilia in a family. Use the pedigree to answer the question that follows. 7. Which type of inheritance pattern is associated with hemophilia? A. autosomal recessive B. sex-linked dominant C. sex-linked recessive D. autosomal dominant

16 Chapter 12 Short Response
Standardized Test Prep Short Response Consider a couple about to get married. The woman has cystic fibrosis, but the man does not. What benefit would they gain by seeing a genetic counselor?

17 Short Response, continued
Chapter 12 Standardized Test Prep Short Response, continued Consider a couple about to get married. The woman has cystic fibrosis, but the man does not. What benefit would they gain by seeing a genetic counselor? Answer: Genetic counseling will tell them the likelihood of each of their children having cystic fibrosis or carrying the cystic fibrosis gene.

18 Chapter 12 Extended Response
Standardized Test Prep Extended Response Colorblindness is a recessive, sex-linked trait. A woman and a man, both with normal vision, have three daughters with normal vision. One of the daughters marries a man with normal vision, and they have a son who is colorblind. Part A Which parent of the son is the carrier of the trait? Explain your answer. Part B What is the likelihood that the children of a woman heterozygous for colorblindness and colorblind man will express the trait? Explain your answer.

19 Extended Response, continued
Chapter 12 Standardized Test Prep Extended Response, continued Answer: Part A The son’s mother carries the trait. The gene for colorblindness is carried on the X chromosome. Part B Given: X-linked recessive: heterozygous female = XB (normal)Xb (colorblind); colorblind male = Xb (colorblind)Y. This Punnett square predicts that 50 percent of the children will be male and 50 percent of the children will be female. 50 percent will be colorblind and 50 percent will have normal vision. 25 percent will be males with normal vision and will not be carriers. 25 percent will be female carriers with normal vision. 25 percent will be colorblind females. 25 percent will be colorblind males.


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