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Genetics Practice Test Date: Name: 1. Which statement best describes a cloned population? 2. A. It is usually produced by sexual reproduction. B. The individual organisms usually have varying DNA sequences. C. There are usually no variations in genotypes. Select the term, chosen from the list below, that is best described by the statement shown. A portion of a chromosome is lost. A. Amniocentesis B. Karyotyping C. Deletion D. Translocation D. Individuals usually show a variety of phenotypes. 3. Patient A Name of Genetic Disorder sickle-cell anemia Characteristics of the Disorder deterioration of the nervous system due to accumulation of fatty material B Patient B has the genetic disorder known as A. 4. phenylketonuria B. Tay-Sachs C. Gregor Mendel developed some basic principles of heredity by 5. hemophilia D. color blindness One reason for Mendel's success with genetic studies of garden peas was that he A. crossing pea plants A. used only hybrid pea plants B. cutting o B. used peas with large chromosomes C. breeding fruit ies C. studied large numbers of o spring the tails of mice D. culturing bacteria in a laboratory D. discovered the sources of variations in peas page 1 6. All the heritable genes found in a population constitute the population's 9. A. recessive alleles A. stores food B. chromosome mutations B. transmits genetic information C. homologous structures C. transmits chemical energy D. gene pool 7. D. stores enzymes Which genetic concept was proposed by Mendel? A. chromosome nondisjunction B. independent assortment C. multiple alleles 10. D. sex linkage 8. Knowledge of the structure of DNA is important in the study of life because DNA located on separate sex chromosomes B. members of an allelic pair C. located on the same chromosome A. on homologous pairs of chromosomes B. in a DNA nucleotide C. in organisms that are homozygous D. on nonhomologous chromosomes Two genes are linked if they are A. Allelic pairs of genes are located only 11. D. able to segregate at random page 2 In humans there are 23 pairs of chromosomes. One pair of the 23 are sex chromosomes. The other 22 pairs are known as A. autosomes B. homozygotes C. heterozygotes D. centrosomes Genetics Practice Test 12. CHROMOSOME THAT CARRIES THE DOMINANT ALLELE FOR HEIGHT CHROMOSOME THAT CARRIES THE RECESSIVE ALLELE FOR HEIGHT CHROMOSOME THAT CARRIES THE DOMINANT ALLELE FOR SEED SHAPE CHROMOSOME THAT CARRIES THE RECESSIVE ALLELE FOR SEED SHAPE Which statement correctly describes the location of the alleles for height and seed shape? A. The dominant alleles for height and seed shape are located on the same chromosome. B. The dominant and recessive alleles are located on the same member of a homologous pair of chromosomes. C. The alleles for height are located on a di erent homologous pair of chromosomes than the alleles for seed shape. D. The dominant alleles are located on one pair of homologous chromosomes and the recessive alleles are located on another pair of homologous chromosomes. 13. Which diagram represents those chromosomes that are responsible for the heterozygous genotype for height? A. B. C. page 3 D. Genetics Practice Test 14. Traits that are controlled by genes found on an X-chromosome are said to be A. autosomal dominant B. autosomal recessive C. codominant 16. Which diagram represents a pair of homologous chromosomes? A. D. sex-linked B. C. 15. While working with pea plants, Gregor Mendel observed that some tall plants had yellow seeds while other tall plants had green seeds. This observation is best explained by A. nondisjunction of chromosomes B. linkage of genes C. independent assortment D. D. intermediate inheritance page 4 Genetics Practice Test 17. The diagram shown represents a pair of homologous autosomes. The letters B and b represents genes for a certain trait. These letters also represent A. an allelic pair of genes B. linked genes C. genes for sex determination 19. 20. If an adenine nucleotide is deleted from a nucleotide sequence in a DNA molecule, the result is a A. clone B. C. polypeptide D. hybrid Base your answer(s) to the following question(s) on the information and diagram below and on your knowledge of biology. In cats, gene E produces yellow fur and gene B produces black fur. A cat that inherits both of these genes has patches of yellow and black fur and is known as a calico. The alleles for black or yellow are located on the X-chromosome. The cross X B Y X B X E is illustrated in the square below. D. homozygous genes 18. Yellow male o spring are represented by A mother with type B blood and a father with type A blood have four children, each with a di erent blood type. The best explanation for the occurrence of the four di erent blood types of the children is that blood type is A. only determined by dominant alleles B. determined by multiple alleles C. in uenced by environmental conditions mutation A. 21. D. a sex-linked trait B. 2 C. 3 D. 4 In humans, the gene for polydactyly (having extra ngers or toes) is dominant over the gene for the normal number of digits. If parents who are both homozygous dominant for polydactyly have four children, how many of these children would most likely have extra ngers or toes? A. page 5 1 0 B. 2 C. 3 D. 4 Genetics Practice Test 22. Base your answer(s) to the following question(s) on the pedigree chart below, which shows a history of ear lobe shape, and on your knowledge of biology. 25. A human hereditary disorder that may result in mental retardation is A. phenylketonuria B. hemophilia C. sickle-cell anemia D. albinism The genotype of individual 1 could be 23. 24. A. EE, only B. Ee, only C. ee D. EE or Ee 26. In which hereditary disease do the abnormal hemoglobin molecules di er from normal hemoglobin molecules by only a single amino acid? A. hemophilia B. albinism C. phenylketonuria D. sickle-cell anemia The genotype of individual 2 could be A. EE, only B. Ee, only C. ee D. EE or Ee 27. The charts show human chromosomes arranged in pairs. Which combination of techniques can be used before birth to detect chromosomal abnormalities? A. ultracentrifugation and chromatography B. screening and vaccination C. blood typing and vaccination The chromosome numbered 1 through 22 are known as D. amniocentesis and karyotyping page 6 A. ribosomes B. lysosomes C. centrosomes D. autosomes Genetics Practice Test 28. 29. The preparation of these charts for individuals A and B is known as A. microsurgery B. C. blood typing D. chemical screening 30. karyotyping A change in the sequence of nitrogenous bases in DNA may result in A. a gene mutation B. sex linkage C. polyploidy D. nondisjunction Which genetic disorder in individual A is indicated by the number of chromosomes labeled 21? A. phenylketonuria (PKU) B. Tay-Sachs C. sickle-cell anemia D. Down's syndrome Techniques for Detecting Genetic Disorders 31. (1) Karyotyping (2) Urinalysis (3) Blood Analysis (4) Amniocentesis Which two techniques would most likely be involved in the prenatal detection of Down's syndrome? A. 1 and 2 B. 2 and 3 C. page 7 1 and 4 D. 1 and 3 Genetics Practice Test 32. From which area would uid be removed to detect genetic disorders by amniocentesis? 34. Persons su ering from sickle-cell anemia have abnormally shaped red blood cells. This condition is most likely caused by A. a diet with insu cient iron B. the lack of an enzyme necessary for proper protein metabolism C. the lack of su cient calcium in bones that produce red blood cells D. hemoglobin molecules that do not contain the normal sequence of amino acids A. A B. B C. C D. D 35. 33. Tay-Sachs is a genetic disorder characterized by a deterioration of the A. circulatory system B. nervous system C. excretory system D. endocrine system Select the technique, chosen from the list below, that is best described by the statement shown. This technique is used to withdraw some of the uid and cells surrounding a fetus. A. Amniocentesis B. Cloning C. Genetic engineering 36. D. Karyotyping page 8 An analysis of chromosomes may show the loss of a portion of a chromosome. This type of chromosomal change is known as A. nondisjunction B. an addition C. translocation D. a deletion Genetics Practice Test 37. 38. The individual from whom these chromosomes were taken is a A. male B. C. hermaphrodite D. polyploid 39. female Examination of the diagram indicates that these are the chromosomes of a A. female with Down syndrome B. male with Down syndrome C. female without Down syndrome D. male without Down syndrome The chart represents the inheritance of Tay-Sachs disease in a family. 40. Answer the following question(s) based on the chart shown and on your knowledge of biology. What are the genotypes of individuals A and B with regard to Tay-Sachs disease? A. One must be homozygous dominant and the other must be homozygous recessive. B. One must be homozygous dominant and the other must be heterozygous. C. Both must be homozygous. A trait appears in six out of seven boys in a particular family, but in one of the girls. Which pattern of heredity is suggested by this information? A. incomplete dominance B. multiple alleles C. independent assortment D. sex linkage D. Both must be heterozygous. page 9 Genetics Practice Test Problem-Attic format version 4.4.274 c 2011–2016 EducAide Software _ Licensed for use by Claire Minto Terms of Use at www.problem-attic.com Genetics Practice Test 09/28/2016 1. Answer: C 21. Answer: D 2. Answer: C 22. Answer: D 3. Answer: B 23. Answer: C 4. Answer: A 24. Answer: D 5. Answer: C 25. Answer: A 6. Answer: D 26. Answer: D 7. Answer: B 27. Answer: D 8. Answer: C 28. Answer: B 9. Answer: B 29. Answer: D 10. Answer: A 30. Answer: A 11. Answer: A 31. Answer: C 12. Answer: C 32. Answer: D 13. Answer: A 33. Answer: A 14. Answer: D 34. Answer: D 15. Answer: C 35. Answer: B 16. Answer: B 36. Answer: D 17. Answer: A 37. Answer: A 18. Answer: B 38. Answer: D 19. Answer: B 39. Answer: D 20. Answer: D 40. Answer: D