Human Heredity: Principles and Issues (MindTap Course List)
11th Edition
ISBN: 9781305251052
Author: Michael Cummings
Publisher: Cengage Learning
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Textbook Question
Chapter 4, Problem 20QP
Analysis of X-Linked Dominant and Recessive Traits
The following is a pedigree for a common genetic trait. Analyze the pedigree to determine whether the trait is inherited as:
- a. autosomal dominant
- b. autosomal recessive
- c. X-linked dominant
- d. X-linked recessive
- e. Y-linked
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Please explain I don’t think this is autosomal dominant as female are more affected than male and please explain B part of the question well.
Generation
a. What is the genotype of the mother?
b. What is the genotype of the father?
c. What are the genotypes of the five children"
41. What is/are the possible inheritance pattern(s) for the characteristic in the following pedigree?
11
a. Autosomal recessive only i
b. Autosomal dominant only)
c. X-linked recessive only
d. X-linked dominant only
e. All of the above are possible.
42. What is/are the possible inheritance pattern(s) for the characteristic in the following pedigree?
11
a Autosomal recessive only
b. Autosomal dominant only
c. X-linked recessive only
d X-linked dominant only
e. All of them are possible.
43. If the phenotype followed in the pedigree below is X-linked recessive, then the genotype of 11-2 is
HI
a homozygous dominant
b heterozygous
chomozygous recessive
d hemuzygous dominant
e bemizygous recessive
While studying of the family tree with history of hypertrichosis (hyper hirsutism of
the ear) this sign was founded only in the men and it was inherited from father to
the son. Define the type of hypertrichosis inheritance?
Select one:
a. Y-linked
b.
Autosomal-recessive
O c. Autosomal-dominant
d. Recessive, X-linked
e. Dominant, X-linked
Chapter 4 Solutions
Human Heredity: Principles and Issues (MindTap Course List)
Ch. 4.3 - Does a pedigree drawn from the available...Ch. 4.3 - Prob. 2EGCh. 4.7 - Did the fact that Prince Albert and Queen Victoria...Ch. 4.7 - Which members of the pedigree could have been...Ch. 4 - Pedigree analysis is a fundamental tool for...Ch. 4 - Pedigree analysis is a fundamental tool for...Ch. 4 - Pedigree analysis is a fundamental tool for...Ch. 4 - Pedigree Analysis Is a Basic Method in Human...Ch. 4 - Pedigree Analysis Is a Basic Method in Human...Ch. 4 - Pedigree Analysis Is a Basic Method in Human...
Ch. 4 - Pedigree Analysis Is a Basic Method in Human...Ch. 4 - Analysis of Autosomal Recessive and Dominant...Ch. 4 - Analysis of Autosomal Recessive and Dominant...Ch. 4 - Use the following information to respond to the...Ch. 4 - Analysis of Autosomal Recessive and Dominant...Ch. 4 - Analysis of Autosomal Recessive and Dominant...Ch. 4 - A proband female with an unidentified disease...Ch. 4 - Analysis of Autosomal Recessive and Dominant...Ch. 4 - Prob. 12QPCh. 4 - Analysis of Autosomal Recessive and Dominant...Ch. 4 - Analysis of Autosomal Recessive and Dominant...Ch. 4 - Analysis of X-Linked Dominant and Recessive Traits...Ch. 4 - Prob. 16QPCh. 4 - Analysis of X-Linked Dominant and Recessive Traits...Ch. 4 - Analysis of Autosomal Recessive and Dominant...Ch. 4 - Analysis of X-Linked Dominant and Recessive Traits...Ch. 4 - Analysis of X-Linked Dominant and Recessive Traits...Ch. 4 - Analysis of X-Linked Dominant and Recessive Traits...Ch. 4 - Analysis of X-Linked Dominant and Recessive Traits...Ch. 4 - Prob. 23QPCh. 4 - Prob. 24QPCh. 4 - Variations in Phenotype Expression Define...Ch. 4 - Prob. 26QPCh. 4 - Variations in Phenotype Expression A genetic...Ch. 4 - Variations in Phenotype Expression Explain how...
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- Examine the following pedigrees. Which is the most likely mode of inheritance of each disorder? (a) autosomal recessive (b) autosomal dominant (c) X-linked recessive (d) a, b, or c (e) a or c 10.arrow_forwardAnalysis of Autosomal Recessive and Dominant Traits a. What pattern of inheritance is suggested by the following pedigree? b. For genotype assignment, assume that the pedigree is for an autosomal dominant trait and that the affected male in the first generation is heterozygous. Assign genotypes to all other individuals in the pedigree.arrow_forwardAnalysis of X-Linked Dominant and Recessive Traits Suppose a couple, both phenotypically normal, have two children: one unaffected daughter and one son affected with a genetic disorder. The phenotype ratio is 1:1, making it difficult to determine whether the trait is autosomal or X-linked. With your knowledge of genetics, what are the genotypes of the parents and children in the autosomal case? In the X-linked case?arrow_forward
- Given the following pedigree added. What questions are true and false?arrow_forwardWebbed fingers is inherited as an X-linked disease An unaffected male marries an affected female. a. Draw a Punnett square of the possible offspring. b. List the phenotypes of the possible children c. Draw a pedigree that displays the inheritance in you Punnett squarearrow_forward... .. Answer BOTH Explain will upvotearrow_forward
- Match the descriptions with the appropriate pedigree. Inheritance of a dominant trait Inheritance of a recessive Inheritance of a Inheritance of a X-linked autosomal trait recessive, sex-linked trait trait Pedigree A Pedigree B Pedigree Carrow_forwardAssuming complete penetrance, which type of inheritance pattern isconsistent with the pedigree shown here? a. Autosomal recessiveb. Autosomal dominantc. X-linked recessived. X-linked dominantarrow_forwardPedigree chart *questions are on the image attachedarrow_forward
- A. Identify the pattern of inheritance in the pedigree below. B. Provide two pieces of evidence that you used to come to this conclusion. C. Identify the genotypes of individuals II-1 and III-2 (at the arrows)arrow_forwardGenetic Inheritance Patterms Retinitis pigmnentosa (RP) can be autosomal recessive, autosomal dominant, or x-linked. Apparently the dominant forms are often less severe. Eric's form of RP is Usher's Syndrome, which is an autosomal recessive inheritance (i.e., you must get a copy of the defective gene from your Mom and one from your Dad). Autosomal means it is not carried on one of the chromosomes that determines sex. Usher's Type II is recessive, so for Eric this means that both his Mom and Dad are carriers of this condition. His brother, Dirk, does not have any symptoms of RP. Question below - short answer approach Imagine you are a genetics counselor, and Dirk, Erik's brother, comes in to see you. Based on his parents, what are Dirk's possible genotypes for RP? What advice would you give Dirk about the chances of Dirk's children having retinitis pigmentosa if his wife is not a carrier? How would your advice change if his wife fully has the disease? Describe all the possibilities,…arrow_forward18)arrow_forward
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