Thompson & Thompson Genetics in Medicine Elsevier eBook on VitalSource, 8th Edition

1. Introduction
2. Introduction to the Human Genome
3. The Human Genome: Gene Structure and Function
4. Human Genetic Diversity: Mutation and Polymorphism
5. Principles of Clinical Cytogenetics and Genome Analysis
6. The Chromosomal and Genomic Basis of Disease: Disorders of the Autosomes and Sex Chromosomes
7. Patterns of Single-Gene Inheritance
8. Complex Inheritance of Common Multifactorial Disorders
9. Genetic Variation in Populations
10. Identifying the Genetic Basis for Human Disease
11. The Molecular Basis of Genetic Disease
12. The Molecular, Biochemical, and Cellular Basis of Genetic Disease
13. The Treatment of Genetic Disease
14. Developmental Genetics and Birth Defects
15. Cancer Genetics and Genomics
16. Risk Assessment and Genetic Counseling
17. Prenatal Diagnosis and Screening
18. Application of Genomics to Medicine and Personalized Health Care
19. Ethical and Social Issues in Genetics and Genomics

Robert L. Nussbaum, MD, FACP, FACMG, Holly Smith Chair of Medicine and Science, Professor of Medicine, Neurology, Pediatrics and Pathology, Department of Medicine and Institute for Human Genetics, University of California San Francisco, San Francisco, California, Roderick R. McInnes, CM, MD, PhD, FRS(C), FCAHS, FCCMG, Alva Chair in Human Genetics, Canada Research Chair in Neurogenetics, Professor of Human Genetics and Biochemistry, Director, Lady Davis Institute, Jewish General Hospital, McGill University, Montreal, Quebec, Canada and Huntington F Willard, Chief Scientific Officer, Genome Medical, Inc., South San Francisco, CA, USA