The mode of inheritance for Craniofrontonasal syndrome CFNS on the basis of the given result. Introduction: Craniofrontonasal syndrome occurs due to mutations in the ephrin- B1 (EFNB1) gene. It is an X-linked disorder. In this case, males usually suffer from hypertelorism, and it is an abnormal condition, which increases the distance between two organs. Females suffer from abnormal development of the head and face before birth. In this disease, patients suffer from various other skeletal abnormalities.

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Answer 1

Question

Chapter 4.2, Problem 31AQP

Summary Introduction

To determine:

The mode of inheritance for Craniofrontonasal syndrome CFNS on the basis of the given result.

Introduction:

Craniofrontonasal syndrome occurs due to mutations in the ephrin-B1(EFNB1) gene. It is an X-linked disorder. In this case, males usually suffer from hypertelorism, and it is an abnormal condition, which increases the distance between two organs. Females suffer from abnormal development of the head and face before birth. In this disease, patients suffer from various other skeletal abnormalities.

Summary Introduction

To explain:

The most likely genotype of the parents in family 1 and in family 10a.

Introduction:

Craniofrontonasal syndrome occurs due to mutations in the ephrin-B1(EFNB1) gene. It is an X-linked disorder. In this case, males usually suffer from hypertelorism, and it is an abnormal condition, which increases the distance between two organs. Females suffer from abnormal development of the head and face before birth. In this disease, patients suffer from various other skeletal abnormalities.

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Answer 2

Question

Chapter 4.2, Problem 31AQP

Summary Introduction

To determine:

The mode of inheritance for Craniofrontonasal syndrome CFNS on the basis of the given result.

Introduction:

Craniofrontonasal syndrome occurs due to mutations in the ephrin-B1(EFNB1) gene. It is an X-linked disorder. In this case, males usually suffer from hypertelorism, and it is an abnormal condition, which increases the distance between two organs. Females suffer from abnormal development of the head and face before birth. In this disease, patients suffer from various other skeletal abnormalities.

Summary Introduction

To explain:

The most likely genotype of the parents in family 1 and in family 10a.

Introduction:

Craniofrontonasal syndrome occurs due to mutations in the ephrin-B1(EFNB1) gene. It is an X-linked disorder. In this case, males usually suffer from hypertelorism, and it is an abnormal condition, which increases the distance between two organs. Females suffer from abnormal development of the head and face before birth. In this disease, patients suffer from various other skeletal abnormalities.

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Answer 3

Question

Chapter 4.2, Problem 31AQP

Summary Introduction

To determine:

The mode of inheritance for Craniofrontonasal syndrome CFNS on the basis of the given result.

Introduction:

Craniofrontonasal syndrome occurs due to mutations in the ephrin-B1(EFNB1) gene. It is an X-linked disorder. In this case, males usually suffer from hypertelorism, and it is an abnormal condition, which increases the distance between two organs. Females suffer from abnormal development of the head and face before birth. In this disease, patients suffer from various other skeletal abnormalities.

Summary Introduction

To explain:

The most likely genotype of the parents in family 1 and in family 10a.

Introduction:

Craniofrontonasal syndrome occurs due to mutations in the ephrin-B1(EFNB1) gene. It is an X-linked disorder. In this case, males usually suffer from hypertelorism, and it is an abnormal condition, which increases the distance between two organs. Females suffer from abnormal development of the head and face before birth. In this disease, patients suffer from various other skeletal abnormalities.

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Answer 4

Question

Chapter 4.2, Problem 31AQP

Summary Introduction

To determine:

The mode of inheritance for Craniofrontonasal syndrome CFNS on the basis of the given result.

Introduction:

Craniofrontonasal syndrome occurs due to mutations in the ephrin-B1(EFNB1) gene. It is an X-linked disorder. In this case, males usually suffer from hypertelorism, and it is an abnormal condition, which increases the distance between two organs. Females suffer from abnormal development of the head and face before birth. In this disease, patients suffer from various other skeletal abnormalities.

Summary Introduction

To explain:

The most likely genotype of the parents in family 1 and in family 10a.

Introduction:

Craniofrontonasal syndrome occurs due to mutations in the ephrin-B1(EFNB1) gene. It is an X-linked disorder. In this case, males usually suffer from hypertelorism, and it is an abnormal condition, which increases the distance between two organs. Females suffer from abnormal development of the head and face before birth. In this disease, patients suffer from various other skeletal abnormalities.

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Answer 5

Chapter 4.2, Problem 31AQP

Summary Introduction

To determine:

The mode of inheritance for Craniofrontonasal syndrome CFNS on the basis of the given result.

Introduction:

Craniofrontonasal syndrome occurs due to mutations in the ephrin-B1(EFNB1) gene. It is an X-linked disorder. In this case, males usually suffer from hypertelorism, and it is an abnormal condition, which increases the distance between two organs. Females suffer from abnormal development of the head and face before birth. In this disease, patients suffer from various other skeletal abnormalities.

Summary Introduction

To explain:

The most likely genotype of the parents in family 1 and in family 10a.

Introduction:

Craniofrontonasal syndrome occurs due to mutations in the ephrin-B1(EFNB1) gene. It is an X-linked disorder. In this case, males usually suffer from hypertelorism, and it is an abnormal condition, which increases the distance between two organs. Females suffer from abnormal development of the head and face before birth. In this disease, patients suffer from various other skeletal abnormalities.

Answer 6

Chapter 4.2, Problem 31AQP

Summary Introduction

To determine:

The mode of inheritance for Craniofrontonasal syndrome CFNS on the basis of the given result.

Introduction:

Craniofrontonasal syndrome occurs due to mutations in the ephrin-B1(EFNB1) gene. It is an X-linked disorder. In this case, males usually suffer from hypertelorism, and it is an abnormal condition, which increases the distance between two organs. Females suffer from abnormal development of the head and face before birth. In this disease, patients suffer from various other skeletal abnormalities.

Answer 7

Chapter 4.2, Problem 31AQP

Summary Introduction

To determine:

The mode of inheritance for Craniofrontonasal syndrome CFNS on the basis of the given result.

Introduction:

Craniofrontonasal syndrome occurs due to mutations in the ephrin-B1(EFNB1) gene. It is an X-linked disorder. In this case, males usually suffer from hypertelorism, and it is an abnormal condition, which increases the distance between two organs. Females suffer from abnormal development of the head and face before birth. In this disease, patients suffer from various other skeletal abnormalities.

Answer 8

Summary Introduction

To explain:

The most likely genotype of the parents in family 1 and in family 10a.

Introduction:

Craniofrontonasal syndrome occurs due to mutations in the ephrin-B1(EFNB1) gene. It is an X-linked disorder. In this case, males usually suffer from hypertelorism, and it is an abnormal condition, which increases the distance between two organs. Females suffer from abnormal development of the head and face before birth. In this disease, patients suffer from various other skeletal abnormalities.

Answer 9

Summary Introduction

To explain:

The most likely genotype of the parents in family 1 and in family 10a.

Introduction:

Craniofrontonasal syndrome occurs due to mutations in the ephrin-B1(EFNB1) gene. It is an X-linked disorder. In this case, males usually suffer from hypertelorism, and it is an abnormal condition, which increases the distance between two organs. Females suffer from abnormal development of the head and face before birth. In this disease, patients suffer from various other skeletal abnormalities.

Answer 10

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Answer 11

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Answer 12

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Answer 13

Ch. 4.1 - Prob. 1CC Ch. 4.1 - Prob. 2CC Ch. 4.1 - Prob. 3CC Ch. 4.1 - Prob. 4CC Ch. 4.1 - Prob. 1COQ Ch. 4.1 - Prob. 2COQ Ch. 4.1 - Prob. 3COQ Ch. 4.1 - Prob. 4COQ Ch. 4.1 - Prob. 5COQ Ch. 4.1 - Prob. 6COQ

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