Genetics: Analysis and Principles
6th Edition
ISBN: 9781259616020
Author: Robert J. Brooker Professor Dr.
Publisher: McGraw-Hill Education
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Chapter 8, Problem 14CONQ
Summary Introduction
Introduction:
Mutations are any permanent changes or alterations in the genetic material. There are different types of mutations, which may lead to changes in the chromosome such as duplication, deletion, inversion, and translocation. Some of these mutations alter the amount of genetic material and may result in
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In a karyotype of a man whose wife has had several miscarriages, it was discovered that he had onlv 45 chromosomes. However, he displayed no obvious phenotypic defects. Furthermore, one of the chromosomes of pair 15 was abnormally long. Which of the following terms best describes the condition of this man?
a. monosomy
b,. trisomy
c. tetrasomy
d. translocation carrier
e. edward syndorme
During the pathoanatomic inspection of a baby-boy's dead body the following abnormalities: polydactily, microcephaly, a cleft
lip and cleft palate, hypertrophy of the parenchymal organs were found. These symptoms are typical of Patau syndrome. What
is the cause of this disease?
Select one:
a. Trisomy on the 21st chromosome.
O b. Trisomy on the 18th chromosome.
c. Trisomy on the 13th chromosome.
d. Trisomy on X chromosome.
e. Monosomy on X chromosome.
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a. Williams Syndrome
b. Cri-Du-Chat Syndrome
c. Pallister-Killian Syndrome
d. Wolf-Hirschhorn Syndrome
1. Caused by a deletion in chromosome 5.
2. Has bulging, wide-set eyes.
3. Has hypertelorism.
4. Caused by an isochromosome.
5. Caused by the deletion of multiple genes on chromosome 7.
6. About 30% of the people with this disorder are autistic.
7. They have an elf-like face.
8. Has a high chance of having scoliosis.
9. White starburst pattern around the iris
Chapter 8 Solutions
Genetics: Analysis and Principles
Ch. 8.1 - 1. A chromosome that is metacentric has its...Ch. 8.1 - Staining eukaryotic chromosomes is useful because...Ch. 8.2 - Prob. 1COMQCh. 8.3 - Which of the following statements is correct? a....Ch. 8.3 - Prob. 2COMQCh. 8.4 - 1. A paracentric inversion
a. includes the...Ch. 8.4 - Due to crossing over within an inversion loop, a...Ch. 8.4 - 3. A mechanism that may cause a translocation is...Ch. 8.5 - 1. Humans have 23 chromosomes per set. A person...Ch. 8.6 - Prob. 1COMQ
Ch. 8.6 - Prob. 2COMQCh. 8.7 - The term endopolyploidy refers to the phenomenon...Ch. 8.7 - 2. In agriculture, an advantage of triploidy in...Ch. 8.8 - Prob. 1COMQCh. 8.8 - The somatic cells of an allotetraploid contain a....Ch. 8 - 1. Which changes in chromosome structure cause a...Ch. 8 - Prob. 2CONQCh. 8 - 3. How does a chromosomal duplication occur?
Ch. 8 - 4. What is a gene family? How are gene families...Ch. 8 - Prob. 5CONQCh. 8 - Two chromosomes have the following orders for...Ch. 8 - An inversion heterozygote has the following...Ch. 8 - Prob. 8CONQCh. 8 - Explain why inversions and reciprocal...Ch. 8 - 10. An individual has the following reciprocal...Ch. 8 - A phenotypically normal individual has the...Ch. 8 - 12. Two phenotypically normal parents produce a...Ch. 8 - With regard to the segregation of centromeres, why...Ch. 8 - Prob. 14CONQCh. 8 - Prob. 15CONQCh. 8 - 16. A phenotypically abnormal individual has a...Ch. 8 - 17. A diploid fruit fly has eight chromosomes. How...Ch. 8 - Prob. 18CONQCh. 8 - Prob. 19CONQCh. 8 - 20. Aneuploidy is typically detrimental, whereas...Ch. 8 - 21. Explain how aneuploidy, deletions, and...Ch. 8 - Prob. 22CONQCh. 8 - 23. A cytogeneticist has collected tissue samples...Ch. 8 - Prob. 24CONQCh. 8 - A zookeeper has collected a male and a female...Ch. 8 - Prob. 26CONQCh. 8 - 27. What is mosaicism? How is it produced?
Ch. 8 - 28. Explain how polytene chromosomes of Drosophila...Ch. 8 - 29. Describe some of the advantages of polyploid...Ch. 8 - 30. While conducting field studies on a chain of...Ch. 8 - Prob. 31CONQCh. 8 - Which of the following terms should not be used to...Ch. 8 - Prob. 33CONQCh. 8 - Prob. 34CONQCh. 8 - A triploid plant has 18 chromosomes (i.e., 6...Ch. 8 - Prob. 36CONQCh. 8 - Prob. 37CONQCh. 8 - 38. A woman who is heterozygous, Bb, has brown...Ch. 8 - 39. What is an allodiploid? What factor determines...Ch. 8 - Prob. 40CONQCh. 8 - 41. Table 8.1 shows that Turner syndrome occurs...Ch. 8 - 42. Male honeybees, which are haploid, produce...Ch. 8 - Prob. 1EQCh. 8 - Prob. 2EQCh. 8 - With regard to the analysis of chromosome...Ch. 8 - 4. Describe how colchicine can be used to alter...Ch. 8 - 5. Describe the steps you would take to produce a...Ch. 8 - Prob. 6EQCh. 8 - What are G bands? Discuss how G bands are useful...Ch. 8 - A female fruit fly has one normal X chromosome and...Ch. 8 - Prob. 2QSDCCh. 8 - Besides the ones mentioned in this textbook, look...Ch. 8 - Prob. 4QSDCCh. 8 - 5. Discuss the importance of gene families at the...
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- A man who is a carrier of a translocated 15/21 chromosome marries a genotypically normal woman. a. Show the possible gametes that will be formed by this man if the translocated 15/21 chromosome synapses with chromosome 21 at Prophase I.arrow_forwardA young couple is planning to have children. Knowing that there have been a substantial number of stillbirths, miscarriages, and fertility problems on the husband’s side of the family, they see a genetic counselor. A chromosome analysis reveals that, whereas the woman has a normal karyotype, the man possesses only 45 chromosomes and is a carrier of a Robertsonian translocation between chromosomes 22 and 13. a. List all the different types of gametes that might be produced by the man. b. What types of zygotes will develop when each of gametes produced by the man fuses with a normal gamete produced by the woman? c. If trisomies and monosomies entailing chromosomes 13 and 22 are lethal, approximately what proportion of the surviving offspring are expected to be carriers of the translocation?arrow_forwardWhen n equals ABC, AAAABBBBCCCC is: a. trisomic b. tetraploid c. tetrasomic d. triploidarrow_forward
- List the diagnostic features (genetic or cytological) that are used to identify these chromosomal alterations:a. Deletionsb. Duplicationsarrow_forwardAltered chromosome structure can drastically affect an individual organism’s phenotype. However, some types of chromosomal rearrangements are more likely to be harmful than others. Categorize the following types of rearrangements from MOST LIKELY to be harmful to LEAST LIKELY to be harmful. A. reciprocal translocation, deletion, translocation B. deletion, translocation, inversion C. inversion, translocation, reciprocal translocation D. translocation, inversion, duplicationarrow_forwardAn individual is heterozygous for a reciprocal translocation, with the following chromosomes: A • B C D E F A • B C V W X R ST • U D E F R ST • U V W X Q. Explain why the fertility of this individual is likely to be less than the fertility of an individual without a translocation.arrow_forward
- An individual is heterozygous for a reciprocal translocation, with the following chromosomes: A • B C D E F A • B C V W X R S T • U D E F R S T • U V W X a. Draw a picture of these chromosomes pairing in prophase I of meiosis. b. Draw the products of alternate, adjacent-1, and adjacent-2 segregations. c. Explain why the fertility of this individual is likely to be less than the fertility of an individual without a translocation.arrow_forwardSpecies I has 2 n = 16 chromosomes. How many chromosomes will be found per cell in each of the following mutants in this species? a. Monosomic b. Autotriploid c. Autotetraploid d. Trisomic e. Double monosomic f. Nullisomic g. Autopentaploid h. Tetrasomicarrow_forwardAn individual heterozygous for a reciprocal translocation possesses the following chromosomes: A B • C D E F G A B • C D V W X R S • T U E F G R S • T U V W X a. Draw the pairing arrangement of these chromosomes in prophase I of meiosis. b. Diagram the alternate, adjacent-1, and adjacent-2 segregation patterns in anaphase I of meiosis. c. Give the products that result from alternate, adjacent-1, and adjacent-2 segregation.arrow_forward
- Possible options include: A. Pericentric inversion B. Chromosome duplication C. Trisomy D. Robertsonian translocationarrow_forwardIn a sample of 1000 patients with Down syndrome, a geneticist discovers that 95% of them are trisomic, while 5% have diploid number of chromosomes. Explain this discrepancy.arrow_forwardHow many chromosomes are there in the somatic cells of a newborn boy with: a. The cri-du chat syndrome b. Klinefelter syndrome c. Down syndrome due to a 14/21 Robertsonian translocation d. Triploidy e. Edwards syndromearrow_forward
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