HUMAN BIOLOGY: CONCEPTS - 9780134312729
8th Edition
ISBN: 2819260095972
Author: Johnson
Publisher: PERUSALL
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
![Check Mark](/static/check-mark.png)
Want to see the full answer?
Check out a sample textbook solution![Blurred answer](/static/blurred-answer.jpg)
Students have asked these similar questions
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.
In this image of the human karyotype:
A. The sister chromatids have separated
B. There are 46 pairs of chromosomes
C. The DNA has already been replicated
D. There are 23 pairs of autosomes
E. None are true.
List the diagnostic features (genetic or cytological) that are used to identify these chromosomal alterations:a. Deletionsb. Duplications
Chapter 19 Solutions
HUMAN BIOLOGY: CONCEPTS - 9780134312729
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
- A patient has mental deficiency, a short stature, and the mongolian type of the eyelid fold. The microscopical examination of the patient's karyotype revealed the presence of trisomy on the 21-st chromosome. What do we call the disease which is caused by this chromosomal abnormality? Select one: a. Down's syndrome. b. Klinefelter's syndrome. O c. Turner's syndrome. d. Edward's syndrome. e. Patau syndrome.arrow_forwardPart of the karyotype of a diploid individual who is heterozygous for one chromosomal rearrangement is shown in the diagram. The chromosomes involved in the rearrangement, and their homologous pair, are shown. The location of each gene is labeled using horizontal lines and the name of each gene is labeled using letters or numbers. Answer the following questions about the diagram. A. What rearrangement is shown? Be as specific as possible. B. Describe a mutation scenario that could cause this rearrangement to be formed. A B D E F G H IXI A B с D E IIXDD 1 2 3 4 5 6 F G H D 1 2 34 5 6 Xarrow_forwardGiven the karyotype shown at right, is this a male or a female? Normal or abnormal? What would the phenotype of this individual be?arrow_forward
- 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 syndormearrow_forwarda. What is the diploid number of chromosomes for a human? b. What is the haploid number of chromosomes for a human? Which cells are considered diploid, gametes or somatic cells? C. d. Which cells are considered haploid, gametes or somatic cells?arrow_forward1. The figure below represents a karyotype performed on a somatic cell of an unknown organism. Answer the following questions using the figure. a. Circle (and label) 3 different sets of homologous chromosomes? b. This individual is heterozygote for gene A (Aa), Homozygote recessive for gene B (bb) and gene homozygote dominant for gene c (CC). Also, gene B and gene C are linked. Using the homologous chromosomes you circled in part a), provide a representation of the location of the A, B and C, genes and alleles on the homologous chromosomes and sister chromatids in such a way that is consistent with the scenario described above in part b). Choose the chromosomes of your liking to show an appropriate representation. TMIID IL MIarrow_forward
- Give typing answer with explanation and conclusion to all parts The chromosomes drawn below are found in a human skin cell. The lines represent the chromosomes themselves. The letters indicate the location of a particular version of a gene. a) T/F An individual’s offspring are more likely to inherit a D1 and R together than a D1 and T9 together. b) T/F About 50% of the egg cells from this individual will have both T9 and BA5. c) T/F Because r is recessive, the frequency at which the r version of the gene occurs in a population is lower than the frequency at which the R version occurs in the population. d) T/F If the protein produced by the BA gene is involved in the formation of ovaries, then the BA gene is likely located on a sex chromosome. e) T/F Because the genes shown here are found in skin cells, these genes code for proteins required for skin cell function.arrow_forwardDiscuss 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_forward3) A. How are the following proteins involved in cell division: condensing, cohesin, kinetochore complex, tubulin? B. Why does phenotype not always reveal genotype? C. How can Mendel's postulates of segregation and independent assortment be explained by meiosis? D. Explain the genotypic and phenotypic ratios predicted when performing a monohybrid and a dihybrid cross of heterozygotes? E. How can you use the product rule and sum rule to calculate the probability of a particular genotype resulting from crossing parents of specific genotypes?arrow_forward
- Q1: Choose the correct answer of the following questions 1) Which can a chromosome map show? A) the sex of the individual B) the position of genes on a chromosome C) the presence of mutant alleles D) whether a gene is autosomal or recessivearrow_forwardA diploid species has 3 pairs of chromosomes in the somatic cells. In males, the first pair is large submetacentric; the second is medium acrocentric, and the third is small telocentric. In females, the first two pairs are like those of the males while the third is large metacentric with satellite. Illustrate the karyograms of the following: a. A triploid cell in femalesb. tetrasomic cell in malesc. tetraploid cell in femalesarrow_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 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_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
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305251052/9781305251052_smallCoverImage.gif)
Human Heredity: Principles and Issues (MindTap Co...
Biology
ISBN:9781305251052
Author:Michael Cummings
Publisher:Cengage Learning