Emery's Elements of Medical Genetics

Höfundar: Peter D Turnpenny; Sian Ellard; Ruth Cleaver (Útgáfa: 16)
Emery's Elements of Medical Genetics

Kaup valmöguleikar

Long recognized as a leading textbook in this fast-moving field, Emery's Elements of Medical Genetics and Genomics offers current, complete information with a strong basis in practical clinical genetics and genomics for medical school and beyond. The 16th Edition of this award-winning text has been thoroughly updated throughout and includes case-based and multiple-choice questions, end-of-chapter summaries, an extensive glossary, and convenient online access, making it an ideal choice for all medical undergraduates as well as postgraduates seeking to improve their understanding and knowledge.

Includes new case-based studies with questions and answers throughout, in addition to multiple-choice self-assessment questions for study and review. Covers key topics such as pharmacogenetics, personalized medicine, prenatal testing, reproductive genetics, and ethical and legal issues in medical genetics. Divides the text into three easy-to-use sections: The Scientific Basis of Human Genetics, Genetics in Medicine and Genomic Medicine, and Clinical Genetics, Counseling and Ethics.

Features full-color illustrations and other images that help readers visualize the appearance of genetic disorders and assist with the understanding of complex genetic structures. Contains learning features such as summary boxes, an extensive glossary of terms, online hyperlinks to important genetics websites and clinical databases, and more. Presents the extensive knowledge and experience of distinguished editors Peter D.

Nánar um bókina

Útgefandi
Elsevier Limited (UK)
ISBN
9780702079672
Print ISBN
9780702079665
Format
ePub
Útgáfa
16
Höfundar
Peter D Turnpenny; Sian Ellard; Ruth Cleaver
Tungumál
English
Útgefið
2020-12-15
Prent takmörkun á líftíma
10

Kaflar

  • Cover image
  • Title page
  • Table of Contents
  • Title page
  • Copyright
  • Contents
  • Preface
  • Acknowledgments
  • Dedication
  • List of Illustrations
  • List of Tables
  • Chapter 1: The History and Impact of Genetics in Medicine
  • Section A: The Scientific Basis of Human Genetics
  • Chapter 2: The Cellular and Molecular Basis of Inheritance
  • Chapter 3: Chromosomes and Cell Division
  • Chapter 4: Finding the Cause of Monogenic Disorders by Identifying Disease Genes
  • Chapter 5: Laboratory Techniques for Diagnosis of Monogenic Disorders
  • Chapter 6: Patterns of Inheritance
  • Chapter 7: Population and Mathematical Genetics
  • Chapter 8: Risk Calculation
  • Chapter 9: Developmental Genetics
  • Section B: Genetics in Medicine and Genomic Medicine
  • Chapter 10: Common Disease, Polygenic, and Multifactorial Genetics
  • Chapter 11: Screening for Genetic Disease
  • Chapter 12: Hemoglobin and the Hemoglobinopathies
  • Chapter 13: Immunogenetics
  • Chapter 14: The Genetics of Cancer…and Cancer Genetics
  • Chapter 15: Pharmacogenomics, Precision Medicine, and the Treatment of Genetic Disease
  • Section C: Clinical Genetics, Counseling, and Ethics
  • Chapter 16: Congenital Abnormalities, Dysmorphic Syndromes, and Intellectual Disability
  • Chapter 17: Chromosome Disorders
  • Chapter 18: Inborn Errors of Metabolism
  • Chapter 19: Mainstream Monogenic Disorders
  • Chapter 20: Prenatal Testing and Reproductive Genetics
  • Chapter 21: Genetic Counseling
  • Chapter 22: Ethical and Legal Issues in Medical Genetics
  • Glossary
  • Appendix: Websites and Clinical Databases
  • Multiple-Choice Questions
  • Case-Based Questions
  • Multiple-Choice Answers
  • Case-Based Answers and Discussion
  • Clinical Scenario Answers and Discussion
  • Index