Introduction to Genetic Analysis
11th Edition
ISBN: 9781464109485
Author: Anthony J.F. Griffiths, Susan R. Wessler, Sean B. Carroll, John Doebley
Publisher: W. H. Freeman
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Chapter 4, Problem 63P
Summary Introduction
To determine: The information that can be given to the woman 4 and 5 from generation III about the likelihood of their having sons with hemophilia.
Introduction: Genetic testing is one of the most useful tools in diagnostics to identify genetic abnormalities. It helps to detect the presence of any heritable malformation carried through the genetic makeup of the parents to the offspring.
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Students have asked these similar questions
In a paternity suit, a woman with type O blood claims that a man with type AB blood is the father of her type O baby. List the genetypes of the mom, man, and baby. Can the woman prove he is the father or can he is not? Why or why not? If the accused man was type A insyead of type AB, what would be his possible genotypes? Could the woman prove he is the father? Can the man prove he is not the father? Why or why not?
Please consider the pedigree below. There are no cases of false paternity.
I
II
III
IV
в
1
a. Which individual/s definitely has/have Bombay phenotype in the descendants of I-1 and I-2?
b. What are the genotypes of individuals II-2 and III-2 at the AB0 and H loci?
Please label your answers a and b, Il-2: and Ill-2:.
Assuming both hemophilia and red-green colorblindness are rare traits, who is recombinant in
generation III? (Select all that apply.)
Male
甲
Female
I Hemophilia A
O Hemophilia B
%3D
Color-blind
Hemophilic and
color-blind
None
IlII-3 male
III-1 male
III-2 male
III-4 male
Chapter 4 Solutions
Introduction to Genetic Analysis
Ch. 4 - Prob. 1PCh. 4 - Prob. 5PCh. 4 - Prob. 12PCh. 4 - Prob. 13PCh. 4 - Prob. 14PCh. 4 - Prob. 15PCh. 4 - Prob. 16PCh. 4 - Prob. 17PCh. 4 - Prob. 18PCh. 4 - Prob. 19P
Ch. 4 - Prob. 20PCh. 4 - Prob. 21PCh. 4 - Prob. 21.1PCh. 4 - Prob. 21.2PCh. 4 - Prob. 21.3PCh. 4 - Prob. 21.4PCh. 4 - Prob. 21.5PCh. 4 - Prob. 21.6PCh. 4 - Prob. 21.7PCh. 4 - Prob. 21.8PCh. 4 - Prob. 21.9PCh. 4 - Prob. 21.10PCh. 4 - Prob. 21.11PCh. 4 - Prob. 21.12PCh. 4 - Prob. 21.13PCh. 4 - Prob. 21.14PCh. 4 - Prob. 21.15PCh. 4 - Prob. 21.16PCh. 4 - Prob. 21.17PCh. 4 - Prob. 21.18PCh. 4 - Prob. 21.19PCh. 4 - Prob. 21.20PCh. 4 - Prob. 21.21PCh. 4 - Prob. 21.22PCh. 4 - Prob. 21.23PCh. 4 - Prob. 21.24PCh. 4 - Prob. 21.25PCh. 4 - Prob. 21.26PCh. 4 - Prob. 22PCh. 4 - Prob. 23PCh. 4 - Prob. 24PCh. 4 - Prob. 25PCh. 4 - Prob. 26PCh. 4 - Prob. 27PCh. 4 - Prob. 28PCh. 4 - Prob. 29PCh. 4 - Prob. 30PCh. 4 - Prob. 31PCh. 4 - Prob. 32PCh. 4 - Prob. 33PCh. 4 - Prob. 34PCh. 4 - Prob. 35PCh. 4 - Prob. 36PCh. 4 - Prob. 37PCh. 4 - Prob. 38PCh. 4 - Prob. 38.1PCh. 4 - Prob. 38.2PCh. 4 - Prob. 38.3PCh. 4 - Prob. 38.4PCh. 4 - Prob. 38.5PCh. 4 - Prob. 38.6PCh. 4 - Prob. 38.7PCh. 4 - Prob. 38.8PCh. 4 - Prob. 38.9PCh. 4 - Prob. 38.10PCh. 4 - Prob. 38.11PCh. 4 - Prob. 38.12PCh. 4 - Prob. 38.13PCh. 4 - Prob. 38.14PCh. 4 - Prob. 38.15PCh. 4 - Prob. 38.16PCh. 4 - Prob. 38.17PCh. 4 - Prob. 38.18PCh. 4 - Prob. 38.19PCh. 4 - Prob. 38.20PCh. 4 - Prob. 38.21PCh. 4 - Prob. 38.22PCh. 4 - Prob. 38.23PCh. 4 - Prob. 38.24PCh. 4 - Prob. 39PCh. 4 - Prob. 40PCh. 4 - Prob. 41PCh. 4 - Prob. 42PCh. 4 - Prob. 43PCh. 4 - Prob. 44PCh. 4 - Prob. 45PCh. 4 - Prob. 46PCh. 4 - Prob. 47PCh. 4 - Prob. 48PCh. 4 - Prob. 49PCh. 4 - Prob. 50PCh. 4 - Prob. 51PCh. 4 - Prob. 52PCh. 4 - Prob. 53PCh. 4 - Prob. 54PCh. 4 - Prob. 55PCh. 4 - Prob. 56PCh. 4 - Prob. 57PCh. 4 - Prob. 58PCh. 4 - Prob. 59PCh. 4 - Prob. 60PCh. 4 - Prob. 62PCh. 4 - Prob. 63PCh. 4 - Prob. 64PCh. 4 - Prob. 65PCh. 4 - Prob. 66PCh. 4 - Prob. 67PCh. 4 - Prob. 68PCh. 4 - Prob. 69P
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- A RFLP is discovered that is linked to the gene for Duchenne’s muscular dystrophy (DMD). DMD is an X-linked, recessive trait. The RFLP is 2 map units from the gene for DMD. Consider the following pedigree and Southern blot using a probe that hybridizes to the RFLP. Which band/s is/are associated with DMD? What is the genotype for individuals 3 and 4? (Remember, this is an X linked disease, so use X’s and Y’s to denote). Individual 9 married a man who does NOT have muscular dystrophy, and she is pregnant. DMD is an X-linked trait. What is the probability for their child to have DMD? An amniocentesis is performed and it is determined that 9’s child in utero has only a 10 kb band that hybridizes to the same probe used above. What can you say about the child now?arrow_forwardn corn, male sterility is controlled by maternal cytoplasmic elements. This phenotype renders the male part of the corn plants (i.e the tassel) unable to produce fertile pollen; the female parts, however, remain receptive to pollination by pollen from male fertile corn plants. However, the presence of a nuclear fertility restorer gene F restores fertility to male sterile lines sing the cardboard chips, simulate the crosses indicated below. Give the genotypes and phenotypes of the offsprings in each cross, and properly label the nucleus and the cytoplasm of each individual in the cross Legend male sterile cytoplasm Male fertile cytoplasm FF nucleus Ff nucleus ff nucleus A. Male sterile female x FF male Explain the phenotype of the offspring B. Male sterile female x Ff male Explain the phenotype of the offspringarrow_forwardIn corn, male sterility is controlled by maternal cytoplasmic elements. This phenotype renders the male part of the corn plants (i.e the tassel) unable to produce fertile pollen; the female parts, however, remain receptive to pollination by pollen from male fertile corn plants. However, the presence of a nuclear fertility restorer gene F restores fertility to male sterile lines Using the cardboard chips, simulate the crosses indicated below. Give the genotypes and phenotypes of the offsprings in each cross, and properly label the nucleus and the cytoplasm of each individual in the cross Legend male sterile cytoplasm Male fertile cytoplasm FF nucleus Ff nucleus ff nucleus A. Male sterile female x FF male Explain the phenotype of the offspring B. Male sterile female x Ff male Explain the phenotype of the offspringarrow_forward
- The Xg cell-surface antigen is coded for by a gene located on the X chromosome. No equivalent gene exists on the Y chromosome. Two codominant alleles of this gene have been identified: Xg1 and Xg2. A woman of genotype Xg2/Xg2 bears children with a man of genotype Xg1/Y, and they produce a son with Klinefelter syndrome of genotype Xg1/Xg2Y. Using proper genetic terminology, briefly explain how this individual was generated. In which parent and in which meiotic division did the mistake occur?arrow_forwardMy Question is what is the probability their first child will have hemophilia and drawn pedigrees for family members with genotypes. My explantion so far: A man has both X and Y chromosomes as sex chromosomes in his body. Here, though the brother of the man is hemophiliac, a man can’t be a carrier of hemophilia. So, it can be said that his chromosome is “XnY”.Here, the “n” stands for “normal”.Though the paternal uncle is hemophiliac, a man cannot be a carrier of hemophilia, his niece will not be a career. So it can be said that the woman is also not a carrier and has the “XnX” chromosome.So, as the mother is not a carrier, their first child does not have a chance of having hemophilia. This can be determined as it is known that there is no hidden carrier of hemophilia in the family.arrow_forwardThree linked loci are evaluated to determine the recombination frequency of the loci. To set up the test cross, an individual that is true breeding dominant for all three phenotypes is crossed with an individual that is true breeding recessive for all three phenotypes. F1 offspring are crossed with individuals that are recessive for all phenotypes. The phenotypic results are shown in the table below. Phenotype Number of Offspring Dominant 1, Dominant 2, Dominant 3 322 Dominant 1, Dominant 2, Recessive 3 82 Recessive 1, Dominant 2, Recessive 3 5 Dominant 1, Recessive 2, Dominant 3 2 Recessive 1, Dominant 2, Dominant 3 28 Recessive 1, Recessive 2, Dominant 3 89 Recessive 1, Recessive 2, Recessive 3 312 Dominant 1, Recessive 2, Recessive 3 25 1. Which two phenotypes are parental? 2. What is the map distance between locus 1 and locus 2? 3. What is the map distance between locus 1 and locus 3? 4. What is the map distance between…arrow_forward
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