Whether the genetic modification of defective alleles of sperm and eggs should be permitted or not. Introduction: “Marfan syndrome” is caused due to mutation in the gene FBN1 that produces a protein called Fibrillin-1. This protein forms microfibrils inside the cells, which support the connective tissues. The defect in this protein causes a lack of strength in the connective tissues of the human body. It is inherited in the form of the autosomal dominant trait.

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Chapter 11.8, Problem 1CT

Summary Introduction

To explain: Whether the genetic modification of defective alleles of sperm and eggs should be permitted or not.

Introduction: “Marfan syndrome” is caused due to mutation in the gene FBN1 that produces a protein called Fibrillin-1. This protein forms microfibrils inside the cells, which support the connective tissues. The defect in this protein causes a lack of strength in the connective tissues of the human body. It is inherited in the form of the autosomal dominant trait.

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Answer 2

Question

Chapter 11.8, Problem 1CT

Summary Introduction

To explain: Whether the genetic modification of defective alleles of sperm and eggs should be permitted or not.

Introduction: “Marfan syndrome” is caused due to mutation in the gene FBN1 that produces a protein called Fibrillin-1. This protein forms microfibrils inside the cells, which support the connective tissues. The defect in this protein causes a lack of strength in the connective tissues of the human body. It is inherited in the form of the autosomal dominant trait.

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Answer 3

Question

Chapter 11.8, Problem 1CT

Summary Introduction

To explain: Whether the genetic modification of defective alleles of sperm and eggs should be permitted or not.

Introduction: “Marfan syndrome” is caused due to mutation in the gene FBN1 that produces a protein called Fibrillin-1. This protein forms microfibrils inside the cells, which support the connective tissues. The defect in this protein causes a lack of strength in the connective tissues of the human body. It is inherited in the form of the autosomal dominant trait.

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Answer 4

Question

Chapter 11.8, Problem 1CT

Summary Introduction

To explain: Whether the genetic modification of defective alleles of sperm and eggs should be permitted or not.

Introduction: “Marfan syndrome” is caused due to mutation in the gene FBN1 that produces a protein called Fibrillin-1. This protein forms microfibrils inside the cells, which support the connective tissues. The defect in this protein causes a lack of strength in the connective tissues of the human body. It is inherited in the form of the autosomal dominant trait.

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Answer 5

Chapter 11.8, Problem 1CT

Summary Introduction

To explain: Whether the genetic modification of defective alleles of sperm and eggs should be permitted or not.

Introduction: “Marfan syndrome” is caused due to mutation in the gene FBN1 that produces a protein called Fibrillin-1. This protein forms microfibrils inside the cells, which support the connective tissues. The defect in this protein causes a lack of strength in the connective tissues of the human body. It is inherited in the form of the autosomal dominant trait.

Answer 6

Chapter 11.8, Problem 1CT

Summary Introduction

To explain: Whether the genetic modification of defective alleles of sperm and eggs should be permitted or not.

Introduction: “Marfan syndrome” is caused due to mutation in the gene FBN1 that produces a protein called Fibrillin-1. This protein forms microfibrils inside the cells, which support the connective tissues. The defect in this protein causes a lack of strength in the connective tissues of the human body. It is inherited in the form of the autosomal dominant trait.

Answer 7

Chapter 11.8, Problem 1CT

Summary Introduction

To explain: Whether the genetic modification of defective alleles of sperm and eggs should be permitted or not.

Introduction: “Marfan syndrome” is caused due to mutation in the gene FBN1 that produces a protein called Fibrillin-1. This protein forms microfibrils inside the cells, which support the connective tissues. The defect in this protein causes a lack of strength in the connective tissues of the human body. It is inherited in the form of the autosomal dominant trait.

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Answer 11

Ch. 11.1 - describe the relationships among chromosomes,...Ch. 11.1 - Prob. 2CYL Ch. 11.2 - distinguish between self-fertilization and...Ch. 11.2 - Prob. 2CYL Ch. 11.3 - Prob. 1TC Ch. 11.3 - Prob. 1CSC Ch. 11.3 - describe the pattern of inheritance of a trait...Ch. 11.3 - Prob. 2CYL Ch. 11.3 - Prob. 3CYL Ch. 11.4 - Can the genotype of a plant grown from a smooth,...

Solution Summary: The author explains that Marfan syndrome is caused due to mutation in the gene FBN1 that produces a protein called Fibrillin-1.

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