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• 1. The History and Impact of Genetics in MedicineSection A: The Scientific Basis of Human Genetics2. The Cellular and Molecular Basis of Inheritance3. Chromosomes and Cell Division4. Finding the Cause of Monogenic Disorders by Identifying Disease Genes5. Laboratory Techniques for Diagnosis of Monogenic Disorders6. Patterns of Inheritance7. Population and Mathematical Genetics8. Risk Calculation9. Developmental GeneticsSection B: Genetics in Medicine and Genomic Medicine10. Common Disease, Polygenic and Multifactorial Genetics11. Screening for Genetic Disease12. Haemoglobin and the Haemoglobinopathies13. Immunogenetics14. The Genetics of Cancer and Cancer Genetics15. Pharmacogenomics, Precision Medicine and the Treatment of Genetic DiseaseSection C: Clinical Genetics, Counselling and Ethics16. Congenital Abnormalities, Dysmorphic Syndromes and Intellectual Disability17. Chromosome Disorders18. Inborn Errors of Metabolism19. Mainstream Monogenic Disorders20. Prenatal Testing and Reproductive Genetics21. Genetic Counselling22. Ethical and Legal Issues in Medical Genetics

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• 1. The History and Impact of Genetics in MedicineSection A: The Scientific Basis of Human Genetics2. The Cellular and Molecular Basis of Inheritance3. Chromosomes and Cell Division4. Finding the Cause of Monogenic Disorders by Identifying Disease Genes5. Laboratory Techniques for Diagnosis of Monogenic Disorders6. Patterns of Inheritance7. Population and Mathematical Genetics8. Risk Calculation9. Developmental GeneticsSection B: Genetics in Medicine and Genomic Medicine10. Common Disease, Polygenic and Multifactorial Genetics11. Screening for Genetic Disease12. Haemoglobin and the Haemoglobinopathies13. Immunogenetics14. The Genetics of Cancer and Cancer Genetics15. Pharmacogenomics, Precision Medicine and the Treatment of Genetic DiseaseSection C: Clinical Genetics, Counselling and Ethics16. Congenital Abnormalities, Dysmorphic Syndromes and Intellectual Disability17. Chromosome Disorders18. Inborn Errors of Metabolism19. Mainstream Monogenic Disorders20. Prenatal Testing and Reproductive Genetics21. Genetic Counselling22. Ethical and Legal Issues in Medical Genetics

Select Guide Rating

• 1. The History and Impact of Genetics in MedicineSection A: The Scientific Basis of Human Genetics2. The Cellular and Molecular Basis of Inheritance3. Chromosomes and Cell Division4. Finding the Cause of Monogenic Disorders by Identifying Disease Genes5. Laboratory Techniques for Diagnosis of Monogenic Disorders6. Patterns of Inheritance7. Population and Mathematical Genetics8. Risk Calculation9. Developmental GeneticsSection B: Genetics in Medicine and Genomic Medicine10. Common Disease, Polygenic and Multifactorial Genetics11. Screening for Genetic Disease12. Haemoglobin and the Haemoglobinopathies13. Immunogenetics14. The Genetics of Cancer and Cancer Genetics15. Pharmacogenomics, Precision Medicine and the Treatment of Genetic DiseaseSection C: Clinical Genetics, Counselling and Ethics16. Congenital Abnormalities, Dysmorphic Syndromes and Intellectual Disability17. Chromosome Disorders18. Inborn Errors of Metabolism19. Mainstream Monogenic Disorders20. Prenatal Testing and Reproductive Genetics21. Genetic Counselling22. Ethical and Legal Issues in Medical Genetics