Genetic Analysis: An Integrated Approach (2nd Edition)
2nd Edition
ISBN: 9780321948908
Author: Mark F. Sanders, John L. Bowman
Publisher: PEARSON
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Textbook Question
Chapter 19, Problem 22P
What is the most likely mode of inheritance for the trait depicted in the following human pedigree?
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a) Which of the four modes of inheritance are consistent with the disease shown in this human pedigrees below? (List the compatible mode or modes) Give an answer for a, b and c
b) If the parents in pedigree c have 2 other children, what is the probability that they will carry the disease?
An unaffected woman for a human disorder marries and unaffected man and they have
children. This results in 3 affected sons, and one unaffected daughter, which ends up having
children later on with an unaffected man and has 2 affected sons.
A) Draw a simple pedigree diagram for this family, including a legend.
B) What is the likely mode of inheritance of this trait: Please explain
C) Provide the genotypes of the original mother and the daughter. Use a capital letter for the
dominant allele and lowercase letter for the recessive allele.
D) If one of the affected sons from the original marriage marries a 2nd cousin that is a carrier of
this trait and has children, what is the probability that they will have 3 affected sons?
The complete absence of one or more teeth (tooth agenesis) is a common trait in humans—indeed, more than 20% of humans lack one or more of their third molars. However, more severe tooth agenesis, defined as the absence of six or more teeth, is less common and is frequently an inherited condition. L. Lammi and colleagues examined tooth agenesis in the Finnish family shown in the pedigree below.
Q.If IV-2 married a man who had a full set of teeth, what is the probability that their child would have tooth agenesis?
Chapter 19 Solutions
Genetic Analysis: An Integrated Approach (2nd Edition)
Ch. 19 - 17.1 Reciprocal crosses of experimental animals or...Ch. 19 - 17.2 How are some of the characteristics of the...Ch. 19 - 17.3 The human mitochondrial genome encodes...Ch. 19 - What is the evidence that transfer of DNA from the...Ch. 19 - Draw a graph depicting the relative amounts of...Ch. 19 - Prob. 6PCh. 19 - 17.7 What is the evidence that the ancient...Ch. 19 - 17.8 Outline the steps required for a gene...Ch. 19 - 17.9 Consider the phylogenetic tree presented in...Ch. 19 - Most large protein complexes in mitochondria and...
Ch. 19 - What insights have analyses of human mitochondrial...Ch. 19 - You are a genetic counselor, and several members...Ch. 19 - A mutation in Arabidopsis immutans results in the...Ch. 19 - What type or types of inheritance are consistent...Ch. 19 - You have isolated (1) a streptomycin-resistant...Ch. 19 - You have isolated two petite mutants, pet1 and...Ch. 19 - 17.15 Consider this human pedigree for a vision...Ch. 19 - A 50- year - old man has been diagnosed with MELAS...Ch. 19 - 17.17 The first person in a family to exhibit...Ch. 19 - Prob. 20PCh. 19 - Prob. 21PCh. 19 - 17.19 What is the most likely mode of inheritance...Ch. 19 - 17.20 In , the Russian Tsar Nicholaswas deposed,...Ch. 19 - 17.21 The dodo bird (Raphus cucullatus) lived on...Ch. 19 - Cytoplasmic male sterility (CMS) in plants has...Ch. 19 - 17.23 Wolves and coyotes can interbreed in...Ch. 19 - Prob. 27PCh. 19 - Prob. 28P
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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
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- A pedigree analysis was performed on the family of a man with schizophrenia. Based on the known concordance statistics, would his MZ twin be at high risk for the disease? Would the twins risk decrease if he were raised in an environment different from that of his schizophrenic brother?arrow_forwardAlbinism in humans is inherited as a simple recessive trait. For the following families, determine the genotypes of the parents and spring. (When two alternative genotypes are possible, list both.) Construct a pedigree of the families in (b) and (c). Suppose that one of the normal children in (b) and one of the albino children in (c) become parents of eight children. Add these children to the pedigree, predicting their phenotypes (normal or albino).arrow_forwardConsider the following pedigree. Solid symbols represent individuals affected by the trait. Assume complete penetrance and non-variable expressivity. II 3 4 III 1 2 3 5 6 a) what is the mode of inheritance of this trait? b) Does the ratio of affected to unaffected offspring in generation III-1 to 1II-4 match the expected ratio for this mode of inheritance? Explain your answer in terms of the expected ratio versus the ratio observed. Give a reason for your answer. No mark is assigned for yes or no)arrow_forward
- Below is a pedigree from one family (two parents and eight children). Four of the children (indicated by shaded shapes) are affected with a serious disease with an unknown genetic cause. a) For the disease, what pattern of inheritance (autosomal/sex-linked, recessive/dominant) is exhibited by this pedigree? b) Linkage analysis of the disease to a series of VNTR polymorphisms on human chromosome 5 is shown above. Is there evidence for linkage between the disorder and the VNTR? Briefly explain your answer.arrow_forwardThe following pedigree illustrates the inheritance of ringed hair, a condition in which each hair is differentiated into light and dark zones. What mode or modes of inheritance are possible for the ringed-hair trait in this family? 2 II 2 3 4 5 6 II 2 3 4 5 IVarrow_forwardIn pedigrees, individuals are usually specified by using a Roman numeral for their generation in the chart and an Arabic number for their position (reading left to right) within that generation. If we use the letter c for the allele that causes cystic fibrosis, what are the genotypes of individuals III-3 and III-4 (the third and fourth individuals shown in generation III) in the pedigree that shows this disease?arrow_forward
- Take the example of B-thalassemia, an autosomal recessive genetic disease that particularly affects people from around the Mediterranean. This disease is associated with an anomaly of hemoglobin, a protein essential for the transport of oxygen, which is composed of four chains: two alpha (a) and two beta (B). In case of B-thalassemia, the ẞ chains are produced in insufficient or no quantity in an individual homozygous recessive resulting in insufficient production of overall hemoglobin leading to anemia and other physiological challenges. The gene that controls the synthesis of the ẞ chains is located on chromosome 11. Here is part of the coding portion of this gene (which controls a total of 146 amino acids and of which you only see the portion 36 to 41) and one of the targeted mutations: 1. Give the sequence of amino acids from the template and mutated strands. 2. What type of point mutation is it? 3. Using the principles of the theory of evolution, explain briefly and generally why…arrow_forwardFor decades scientists have been perplexed by different circumstances surrounding families with rare, early-onset auditory neuropathy (deafness). In some families, parents and grandparents of the proband have normal hearing, while in other families, a number of affected (deaf) family members are scattered throughout the pedigree, appearing in every generation. Assuming a genetic cause for each case, offer a reasonable explanation for the genetic origin of such deafness in the two types of families.arrow_forwardHemophilia is caused by an X-linked recessive mutation in humans. If a woman whose paternal uncle (father's brother) was a hemophiliac marries a man whose brother is also a hemophiliac, what is the probability of their first child having hemophilia (Note: assume that there are no other cases of hemophilia in the pedigree and no hidden carriers)? Select one: a. 1/2 b. 1/8 c. 0 d. 1/4 e. 1 Oarrow_forward
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