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Medical Genetics(医学遗传学)


作者:
丁卫 叶海红
定价:
19.60元
ISBN:
978-7-04-039414-6
版面字数:
260千字
开本:
16开
全书页数:
132页
装帧形式:
平装
重点项目:
暂无
出版时间:
2014-04-18
读者对象:
高等教育
一级分类:
医药
二级分类:
基础医学

Global developments in medicine and health shape trends in medical education. And in China education reform has become an important focus as the country strives to meet the basic requirements for developing a medical education system that meets international standards. Significant medical developments abroad are now being incorporated into the education of both domestic and international-medical students in China, which includes students from the districts of China's Hong Kong, Macao and Taiwan that are taught through mandarin Chinese as well as students from a variety of other regions that are taught through the English language. This latter group creates higher demands for both schools and teachers.

Unfortunately there is no consensus as to how to improve the level and quality of education for these students or even as to which English language materials should be used. Some teachers prefer to directly use original English language materials, while others make use of Chinese medical textbooks with the help of English language medical notes. The lack of consensus has emerged from the lack of English language medical textbooks based on the characteristics of modern medical education in China.

  • 前辅文
  • Chapter 1 Overview of Genetics
    • 1.1 Role of Genetics in Medicine
    • 1.2 Brief History
    • 1.3 Classification of Genetic Disorders
    • 1.4 Future of Medical Genetics
  • Chapter 2 Molecular Basis of Heredity
    • 2.1 DNA Structure and Replication
    • 2.2 Organization of Human Genome
    • 2.3 Gene Expression
    • 2.4 Mutation and Polymorphism
  • Chapter 3 Chromosomal Basis of Heredity
    • 3.1 Characteristics of Human Chromatin and Chromosomes
    • 3.2 Sex Determination
    • 3.3 Variation in Chromosome Number
    • 3.4 Variation in Chromosome Structure
    • 3.5 Disorders of Autosomes and the Sex Chromosome
  • Chapter 4 Single-gene Disorders
    • 4.1 Pedigree and Pedigree Analysis
    • 4.2 Autosomal Dominant Disease
    • 4.3 Autosomal Recessive Disease
    • 4.4 X linked Dominant Genetic Disease
    • 4.5 X linked Recessive Genetic Disease
    • 4.6 Y linked Genetic Disease
    • 4.7 Influencing Factors in the Analysis of Singlegene Disorders
  • Chapter 5 Mitochondrial Inherited Disorders
    • 5.1 Structure, Function and Inheritance of Mitochondria
    • 5.2 Mitochondrial DNA Mutations and Common Mitochondrial Diseases
  • Chapter 6 Multifactorial Genetic Disorders
    • 6.1 Characteristics of Multifactorial Traits
    • 6.2 Inheritance of Multifactorial (Complex) Disorders
    • 6.3 Factors Affecting Estimation of Recurrence Risk for Multifactorial Disorders
  • Chapter 7 Human Biochemical Disorders
    • 7.1 Hemoglobinopathy
    • 7.2 Hemophilia
    • 7.3 Collagen Diseases
    • 7.4 Receptor Protein Disease
    • 7.5 Enzyme Protein Disease
  • Chapter 8 Population Genetics
    • 8.1 Population Genetic Equilibrium
    • 8.2 Factors Affecting Population Genetic Equilibrium
    • 8.3 Genetic Load
  • Chapter 9 Tumor Genetics
    • 9.1 Chromosomal Aberration and Tumors
    • 9.2 Oncogene
    • 9.3 Tumor Suppressor Gene
    • 9.4 Genetic Mechanisms of Tumorigenesis
    • 9.5 Hereditary Malignant Tumors
  • Chapter 10 Diagnosis of Genetic Disorders
    • 10.1 Symptomatic Diagnosis
    • 10.2 Presymptomatic Diagnosis
    • 10.3 Prenatal Diagnosis
  • Chapter 11 Therapy of Hereditary Disease
    • 11.1 General Principles and Concerns
    • 11.2 Surgical, Pharmacological and Dietary Therapy
    • 11.3 Gene Therapy
  • Chapter 12 Prevention of Genetic Disorders
    • 12.1 Genetic Screening
    • 12.2 Genetic Counseling
    • 12.3 Genetic Register

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