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cover image - Thompson & Thompson Genetics in Medicine Elsevier eBook on VitalSource,8th Edition
ISBN: 9780323392044
Copyright: 2016
Publication Date: 05-05-2015
Page Count: 560
Imprint: Elsevier
List Price: $49.99

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

by Robert L. Nussbaum, MD, FACP, FACMG, Roderick R. McInnes, CM, MD, PhD, FRS(C), FCAHS, FCCMG and Huntington F Willard

Elsevier eBook on VitalSource

cover image - Thompson & Thompson Genetics in Medicine Elsevier eBook on VitalSource,8th Edition
ISBN: 9780323392044
Copyright: 2016
Publication Date: 05-05-2015
Page Count: 560
Imprint: Elsevier
List Price: $49.99

$49.99

Or $0.00 with a valid access code

Updated to reflect the newest changes in genetics, Thompson & Thompson's Genetics in Medicine returns as one of the most favored texts in this fascinating and rapidly evolving field. By integrating the classic principles of human genetics with modern molecular genetics, this medical reference book utilizes a variety of learning tools to help you understand a wide range of genetic disorders.

Newer Edition Available

9th Edition

Thompson & Thompson Genetics and Genomics in Medicine Elsevier eBook on VitalSource

Elsevier eBook on VitalSource
ISBN: 9780323553308
    • Acquire the state-of-the-art knowledge you need on the latest advances in molecular diagnostics, the Human Genome Project, pharmacogenetics, and bio-informatics.
    • Better understand the relationship between basic genetics and clinical medicine with a variety of clinical case studies.
    • Recognize a wide range of genetic disorders with visual guidance from more than 240 dynamic illustrations and high-quality photos.
    • Immerse yourself in updated graphics, full-color text, illustrations, line diagrams, and clinical photos of genetic diseases.
    • Explore the latest genetic content available in order to remain up to date on the most current trends in the field.
    • Take advantage of a double-page clinical case study section that demonstrates and reinforces general principles of disease inheritance, pathogenesis, diagnosis, management, and counseling.
    • Enhance your critical thinking skills and better retain information. Each chapter ends with up to 5 quick genetic "problems" related to what has just been reviewed, with answers provided in the back of the book.
    • Student Consult eBook version included with purchase. This enhanced eBook experience allows you to search all of the text, figures, and references from the book on a variety of devices. You'll also access USMLE-style and multiple choice questions.
  • Chapter 1 Introduction

    Chapter 2 Introduction to the Human Genome

    Chapter 3 The Human Genome: Gene Structure and Function

    Chapter 4 Human Genetic Diversity: Mutation and Polymorphism

    Chapter 5 Principles of Clinical Cytogenetics and Genome Analysis

    Chapter 6 The Chromosomal and Genomic Basis of Disease: Disorders of the Autosomes and Sex Chromosomes

    Chapter 7 Patterns of Single-Gene Inheritance

    Chapter 8 Complex Inheritance of Common Multifactorial Disorders

    Chapter 9 Genetic Variation in Populations

    Chapter 10 Identifying the Genetic Basis for Human Disease

    Chapter 11 The Molecular Basis of Genetic Disease

    Chapter 12 The Molecular, Biochemical, and Cellular Basis of Genetic Disease

    Chapter 13 The Treatment of Genetic Disease

    Chapter 14 Developmental Genetics and Birth Defects

    Chapter 15 Cancer Genetics and Genomics

    Chapter 16 Risk Assessment and Genetic Counseling

    Chapter 17 Prenatal Diagnosis and Screening

    Chapter 18 Application of Genomics to Medicine and Personalized Health Care

    Chapter 19 Ethical and Social Issues in Genetics and Genomics

    Cases

  • 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

$49.99

Or $0.00 with a valid access code