The pedigree chart for the whole family. Introduction. The human consists of 23 pairs of chromosomes, condensed form of chromatids which divide during cell division into daughter cells. The human has 22 autosomes and one pair of sex chromosomes. The sex chromosomes determine the sex in an individual based on the type of sex chromosomes that are present in the fusing gametes.

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Answer 1

Question

Chapter 4, Problem 27P

a.

Summary Introduction

To determine: The pedigree chart for the whole family.

Introduction. The human consists of 23 pairs of chromosomes, condensed form of chromatids which divide during cell division into daughter cells. The human has 22 autosomes and one pair of sex chromosomes. The sex chromosomes determine the sex in an individual based on the type of sex chromosomes that are present in the fusing gametes.

b.

Summary Introduction

To determine: The agreement of the pedigree with the hypothesis that Rh+ is dominant allele and Rh- is recessive.

Introduction. The pedigree chart helps to depict the complete history of the pattern of inheritance of genetic disease from one generation to another generation. The inheritable genetic disease is either autosomal dominant or recessive or sex-linked based on which the probability of disease in a future generation can be predicted.

c.

Summary Introduction

To determine: The mechanism of the transmission of elliptocytosis.

Introduction. The dominant allele masks the expression of the recessive allele. Therefore the dominant allele is expressed in homozygous and heterozygous genotype while the recessive phenotype is only expressed under homozygous condition.

d.

Summary Introduction

To determine: The presence of the genes of same chromosome that govern E and Rh phenotypes.

Introduction. Recombination is the process that is exclusive to the meiotic division as it allows the exchange of genetic material between the non-homologous chromosomes. The recombination process is responsible for the shuffling of the characters and producing a zygote that is different from both the parents but have the chromosomes from both the parents.

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A phenotypically normal man, who has a hemophiliac brother, marries a normal woman, who is not a carrier. What is the probability that any of their children will be hemophiliac?

Another couple is concerned their child will be born with sickle cell anemia. The woman does not have sickle cell anemia. The woman’s mother had sickle cell anemia and her father was a carrier of the sickle cell gene. The man knows that he is not a carrier of the sickle cell gene. What is the probability that the child will be a carrier of sickle cell anemia? please include a punnett square

Another couple is concerned their child will be born with sickle cell anemia. The woman does not have sickle cell anemia. The woman’s mother had sickle cell anemia and her father was a carrier of the sickle cell gene. The man knows that he is not a carrier of the sickle cell gene. What is the probability that the child will be a carrier of sickle cell anemia?

Answer 2

Question

Chapter 4, Problem 27P

a.

Summary Introduction

To determine: The pedigree chart for the whole family.

Introduction. The human consists of 23 pairs of chromosomes, condensed form of chromatids which divide during cell division into daughter cells. The human has 22 autosomes and one pair of sex chromosomes. The sex chromosomes determine the sex in an individual based on the type of sex chromosomes that are present in the fusing gametes.

b.

Summary Introduction

To determine: The agreement of the pedigree with the hypothesis that Rh+ is dominant allele and Rh- is recessive.

Introduction. The pedigree chart helps to depict the complete history of the pattern of inheritance of genetic disease from one generation to another generation. The inheritable genetic disease is either autosomal dominant or recessive or sex-linked based on which the probability of disease in a future generation can be predicted.

c.

Summary Introduction

To determine: The mechanism of the transmission of elliptocytosis.

Introduction. The dominant allele masks the expression of the recessive allele. Therefore the dominant allele is expressed in homozygous and heterozygous genotype while the recessive phenotype is only expressed under homozygous condition.

d.

Summary Introduction

To determine: The presence of the genes of same chromosome that govern E and Rh phenotypes.

Introduction. Recombination is the process that is exclusive to the meiotic division as it allows the exchange of genetic material between the non-homologous chromosomes. The recombination process is responsible for the shuffling of the characters and producing a zygote that is different from both the parents but have the chromosomes from both the parents.

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Answer 3

Question

Chapter 4, Problem 27P

a.

Summary Introduction

To determine: The pedigree chart for the whole family.

Introduction. The human consists of 23 pairs of chromosomes, condensed form of chromatids which divide during cell division into daughter cells. The human has 22 autosomes and one pair of sex chromosomes. The sex chromosomes determine the sex in an individual based on the type of sex chromosomes that are present in the fusing gametes.

b.

Summary Introduction

To determine: The agreement of the pedigree with the hypothesis that Rh+ is dominant allele and Rh- is recessive.

Introduction. The pedigree chart helps to depict the complete history of the pattern of inheritance of genetic disease from one generation to another generation. The inheritable genetic disease is either autosomal dominant or recessive or sex-linked based on which the probability of disease in a future generation can be predicted.

c.

Summary Introduction

To determine: The mechanism of the transmission of elliptocytosis.

Introduction. The dominant allele masks the expression of the recessive allele. Therefore the dominant allele is expressed in homozygous and heterozygous genotype while the recessive phenotype is only expressed under homozygous condition.

d.

Summary Introduction

To determine: The presence of the genes of same chromosome that govern E and Rh phenotypes.

Introduction. Recombination is the process that is exclusive to the meiotic division as it allows the exchange of genetic material between the non-homologous chromosomes. The recombination process is responsible for the shuffling of the characters and producing a zygote that is different from both the parents but have the chromosomes from both the parents.

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Answer 4

Question

Chapter 4, Problem 27P

a.

Summary Introduction

To determine: The pedigree chart for the whole family.

Introduction. The human consists of 23 pairs of chromosomes, condensed form of chromatids which divide during cell division into daughter cells. The human has 22 autosomes and one pair of sex chromosomes. The sex chromosomes determine the sex in an individual based on the type of sex chromosomes that are present in the fusing gametes.

b.

Summary Introduction

To determine: The agreement of the pedigree with the hypothesis that Rh+ is dominant allele and Rh- is recessive.

Introduction. The pedigree chart helps to depict the complete history of the pattern of inheritance of genetic disease from one generation to another generation. The inheritable genetic disease is either autosomal dominant or recessive or sex-linked based on which the probability of disease in a future generation can be predicted.

c.

Summary Introduction

To determine: The mechanism of the transmission of elliptocytosis.

Introduction. The dominant allele masks the expression of the recessive allele. Therefore the dominant allele is expressed in homozygous and heterozygous genotype while the recessive phenotype is only expressed under homozygous condition.

d.

Summary Introduction

To determine: The presence of the genes of same chromosome that govern E and Rh phenotypes.

Introduction. Recombination is the process that is exclusive to the meiotic division as it allows the exchange of genetic material between the non-homologous chromosomes. The recombination process is responsible for the shuffling of the characters and producing a zygote that is different from both the parents but have the chromosomes from both the parents.

Expert Solution & Answer

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Answer 5

Chapter 4, Problem 27P

a.

Summary Introduction

To determine: The pedigree chart for the whole family.

Introduction. The human consists of 23 pairs of chromosomes, condensed form of chromatids which divide during cell division into daughter cells. The human has 22 autosomes and one pair of sex chromosomes. The sex chromosomes determine the sex in an individual based on the type of sex chromosomes that are present in the fusing gametes.

b.

Summary Introduction

To determine: The agreement of the pedigree with the hypothesis that Rh+ is dominant allele and Rh- is recessive.

Introduction. The pedigree chart helps to depict the complete history of the pattern of inheritance of genetic disease from one generation to another generation. The inheritable genetic disease is either autosomal dominant or recessive or sex-linked based on which the probability of disease in a future generation can be predicted.

c.

Summary Introduction

To determine: The mechanism of the transmission of elliptocytosis.

Introduction. The dominant allele masks the expression of the recessive allele. Therefore the dominant allele is expressed in homozygous and heterozygous genotype while the recessive phenotype is only expressed under homozygous condition.

d.

Summary Introduction

To determine: The presence of the genes of same chromosome that govern E and Rh phenotypes.

Introduction. Recombination is the process that is exclusive to the meiotic division as it allows the exchange of genetic material between the non-homologous chromosomes. The recombination process is responsible for the shuffling of the characters and producing a zygote that is different from both the parents but have the chromosomes from both the parents.

Answer 6

Chapter 4, Problem 27P

a.

Summary Introduction

To determine: The pedigree chart for the whole family.

Introduction. The human consists of 23 pairs of chromosomes, condensed form of chromatids which divide during cell division into daughter cells. The human has 22 autosomes and one pair of sex chromosomes. The sex chromosomes determine the sex in an individual based on the type of sex chromosomes that are present in the fusing gametes.

Answer 7

Chapter 4, Problem 27P

a.

Summary Introduction

To determine: The pedigree chart for the whole family.

Introduction. The human consists of 23 pairs of chromosomes, condensed form of chromatids which divide during cell division into daughter cells. The human has 22 autosomes and one pair of sex chromosomes. The sex chromosomes determine the sex in an individual based on the type of sex chromosomes that are present in the fusing gametes.

Answer 8

b.

Summary Introduction

To determine: The agreement of the pedigree with the hypothesis that Rh+ is dominant allele and Rh- is recessive.

Introduction. The pedigree chart helps to depict the complete history of the pattern of inheritance of genetic disease from one generation to another generation. The inheritable genetic disease is either autosomal dominant or recessive or sex-linked based on which the probability of disease in a future generation can be predicted.

Answer 9

b.

Summary Introduction

To determine: The agreement of the pedigree with the hypothesis that Rh+ is dominant allele and Rh- is recessive.

Introduction. The pedigree chart helps to depict the complete history of the pattern of inheritance of genetic disease from one generation to another generation. The inheritable genetic disease is either autosomal dominant or recessive or sex-linked based on which the probability of disease in a future generation can be predicted.

Answer 10

c.

Summary Introduction

To determine: The mechanism of the transmission of elliptocytosis.

Introduction. The dominant allele masks the expression of the recessive allele. Therefore the dominant allele is expressed in homozygous and heterozygous genotype while the recessive phenotype is only expressed under homozygous condition.

Answer 11

c.

Summary Introduction

To determine: The mechanism of the transmission of elliptocytosis.

Introduction. The dominant allele masks the expression of the recessive allele. Therefore the dominant allele is expressed in homozygous and heterozygous genotype while the recessive phenotype is only expressed under homozygous condition.

Answer 12

d.

Summary Introduction

To determine: The presence of the genes of same chromosome that govern E and Rh phenotypes.

Introduction. Recombination is the process that is exclusive to the meiotic division as it allows the exchange of genetic material between the non-homologous chromosomes. The recombination process is responsible for the shuffling of the characters and producing a zygote that is different from both the parents but have the chromosomes from both the parents.

Answer 13

d.

Summary Introduction

To determine: The presence of the genes of same chromosome that govern E and Rh phenotypes.

Introduction. Recombination is the process that is exclusive to the meiotic division as it allows the exchange of genetic material between the non-homologous chromosomes. The recombination process is responsible for the shuffling of the characters and producing a zygote that is different from both the parents but have the chromosomes from both the parents.

Answer 14

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Answer 16

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Answer 17

Ch. 4 - Prob. 1P Ch. 4 - Prob. 5P Ch. 4 - Prob. 12P Ch. 4 - Prob. 13P Ch. 4 - Prob. 14P Ch. 4 - Prob. 15P Ch. 4 - Prob. 16P Ch. 4 - Prob. 17P Ch. 4 - Prob. 18P Ch. 4 - Prob. 19P

Solution Summary: The author describes the pedigree chart for the family with Rh antigen and elliptocytosis.

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Chapter 4 Solutions