01 Introduction

1.1 What is Medical Genetics?

Test 1

02 Chromosomal basis of heredity

2.1 Structure of human chromosomes

2.2 Cell division and chromosome

2.3 Karyotype

Test 2

03 Patterns of single-gene inheritance

3.1 Autosomal patterns of Mendelian inheritance

3.2 X-linked inheritance

3.3 Non-Mendelian inheritance

Test 3

04 Principle of clinical cytogenetics

4.1 Methods for chromosome analysis

4.2 Abnormalities of chromosome number

4.3 Structural abnormalities of Chromosome

Test 4

05 Chromosomal Disorder

5.1 Autosomal disorders

5.2 Sex chromosomal disorders

Test 5

06 Multifactorial Disorders

6.1 Qualitative & quantitative traits

6.2 Polygenetic Disease

Test 6

07 Epigenetics

7.1 The phenotype of an organism is the product of interactions between the genome and epigenome

7.2 Epigenetic Alterations to the Genome

7.3 Epigenetics and human diseases

Test 7

08 Genetics of Cancer

8.1 Cancer is fundamentally a genetic disease

8.2 Oncogene and tumor suppressor gene

8.3 Oncogenesis theory

Test 8

09 Genetic variation in individuals and population: Mutation and Polymorphism

9.1 Mutation

9.2 Human genetic diversity

9.3 Genetic variation in populations

Test 9

10 Diagnosis of Genetic Diseases

10.1 A brief history

10.2 Genetic disease and the diagnosis methods

Test 10

11 Genetic counseling and risk assessment

11.1 People involved in genetic counseling

11.2 Genetic counseling process

11.3 Ethical issues

Test 11