HUMAN BIOLOGY W MASTERING BIOLOGY
15th Edition
ISBN: 9781323510803
Author: Johnson
Publisher: PEARSON C
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 19, Problem 14TY
Summary Introduction
Introduction:
A display of all the chromosome of an organism is called karyotype. A karyotype consists of number and appearance of the chromosome in a nucleus. It is used to detect the deviation that occurs in the chromosome. It is also used to check the abnormalities of the chromosome.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
A geneticist determines that the order of four genes on a specific chromosome is CABD because the recombination frequencies were 35% for C-D, 24% for A-D, 23% for B-D, and 10% for A-B. What has the geneticist constructed?
A geneticist determines that the order of four genes on a specific chromosome is CABD because the recombination frequencies were 35% for C-D, 24% for A-D, 23% for B-D, and 10% for A-B. What has the geneticist constructed?
A. a physical map
B. a karyotype
C. a cytogenic map
D. a linkage map
In a college genetics laboratory course, a healthy student constructs a karyotype from a cell from inside her cheek. She finds only one chromosome 3 and one chromosome 21, plus two unusual chromosomes that do not seem to have matching partners.
a. What type of chromosomal abnormality does she have?
b. Why doesn’t she have any symptoms?
c. Would you expect any of her relatives to have particular medical problems?
Chapter 19 Solutions
HUMAN BIOLOGY W MASTERING BIOLOGY
Ch. 19 - If you might be a carrier of a gene for an...Ch. 19 - Prob. 2QCCh. 19 - Prob. 1CRCh. 19 - Prob. 2CRCh. 19 -
3. Distinguish between genotype and phenotype.
Ch. 19 - Describe the contributions of Mendel to the field...Ch. 19 - Explain how alterations of chromosome number and...Ch. 19 - Prob. 6CRCh. 19 - Prob. 7CRCh. 19 - Describe what is meant by sex-linked inheritance.
Ch. 19 -
9. Explain why lethal diseases caused by dominant...Ch. 19 - Prob. 10CRCh. 19 - All of the following statements about homologous...Ch. 19 - Prob. 2TYCh. 19 -
3. Which of the following statements correctly...Ch. 19 - Prob. 4TYCh. 19 - Prob. 5TYCh. 19 - Prob. 6TYCh. 19 - Prob. 7TYCh. 19 - Which of the following results in the separation...Ch. 19 - Prob. 9TYCh. 19 - Prob. 10TYCh. 19 - What tool is used to determine the probabilities...Ch. 19 - Prob. 12TYCh. 19 - What is the basis for the tremendous genetic...Ch. 19 - Prob. 14TYCh. 19 -
15. Which of the following events or processes...Ch. 19 -
1. What fraction of the offspring of two...Ch. 19 -
2. Why is it that the range of resting blood...Ch. 19 - Prob. 3AWKCh. 19 - Geneticists often study patterns of gene transfer...Ch. 19 - Prob. 5AWKCh. 19 - Prob. 6AWKCh. 19 - Nondisjunction during meiosis can lead to the...
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.Similar questions
- Discuss the principles of the chromosome theory of inheritance. Which principles were deducedvia light microscopy, and which were deduced from crosses? What modern techniques couldbe used to support the chromosome theory of inheritance?arrow_forwardIn a human karyotype, chromosomes are arranged in 23 pairs. If one of the autosomal pairs is examined, which of the following characteristics will the two chromosomes of the pair have in common? a) loci and staining pattern b) length and DNA sequence c) X-like shape and alignment on the metaphase plate d) alleles and centromere positionarrow_forwardWhich statement about homologous chromosomes is FALSE? Select one: a. They contain the same genes in the same places along the length of the chromosome b. One member of the homologous pair came from your mother, the other from your father c. For a particular gene, one member of the pair may have one allele, while the other has a different allele d. They are joined together at the centromere as the two halves of the typical X-shaped chromosomearrow_forward
- a. Which progeny are the parental types? How can you tell?b. Which progeny are the recombinants? How can you tell?c. Do the results of this test cross support linkage of the traits? What is the % recombination?arrow_forwardAnswer the following questions: A) Why the extension cannot be 3´---5´ and why it has to be 5´------3´? B) What is a gene?arrow_forwardThe recombinant offspring of the F2 generation were produced bycrossing over that occurreda. during spermatogenesis in the P generation males.b. during oogenesis in the P generation females.c. during spermatogenesis in the F1 males.d. during oogenesis in the F1 females. [Answer the multiple-choice questions based on the following experiment:P generation: True-breeding flies with red eyes and long wings werecrossed to flies with white eyes and miniature wings. All F1 offspringhad red eyes and long wings.The F1 female flies were then crossed to males with white eyes and miniaturewings. The following results were obtained for the F2 generation:129 red eyes, long wings133 white eyes, miniature wings71 red eyes, miniature wings67 white eyes, long wings]arrow_forward
- A research scientist is studying diseases associated with homologous chromosomes and notices that the same gene along the chromosome has different function what can you conclude about his findings? A. The homologous pairs have been recombined and therefore he is studying end joining of chromosomes B. He is studying sex chromosomes and the differences are because the chromosomes are from a male species organism C. He has identified different alleles among homologous chromosomes. D. He is studying basic chromosome remodeling during fertilzationarrow_forwardBoth karyotyping and G_banding techniques show normal chromosomal pattern, however pedigree analysis revealed abnormality of genetic origin, can you think of a reason that would explain the findings?arrow_forwardHow would one explain a testcross involving F1 dihybrid flies in which more parental-type offspring than recombinant-type offspring are produced? Group of answer choices A. The testcross was improperly performed B. The two genes are linked C. Both of the characters are controlled by more than one gene D. The two genes are linked but on different chromosomes E. Recombination did not occur in the cell during meiosisarrow_forward
- A boy with Down syndrome (trisomy 21) has 46 chromosomes. One parent and his two older sisters have a normal phenotype, but each have 45 chromosomes. a)Explain how this is possible. b)How many chromosomes do you expect to see in karyotypes of the parents? c)What term best describes this kind of chromosome abnormality? d)What is the probability the next child of this couple will have a normal phenotype and have 46 chromosomes? Explain your answer.arrow_forwardPedigree Analysis Is a Basic Method in Human Genetics Using the pedigree provided, answer the following questions. a. Is the proband male or female? b. Is the grandfather of the proband affected? c. How many siblings does the proband have, and where is he or she in the birth order?arrow_forwardWhat is shown here? A. Heterotype B. Phenotype C. Karyotype D. Genotypearrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Human Heredity: Principles and Issues (MindTap Co...BiologyISBN:9781305251052Author:Michael CummingsPublisher:Cengage Learning
Human Heredity: Principles and Issues (MindTap Co...
Biology
ISBN:9781305251052
Author:Michael Cummings
Publisher:Cengage Learning