Emery's Elements of Medical Genetics and Genomics

Author:   Peter D Turnpenny, BSc MB ChB DRCOG DCH FRCP FRCPCH FRCPath FHEA (Consultant Clinical Geneticist, Royal Devon and Exeter Hospital<br>Senior Clinical Lecturer, Peninsula Medical School, Exeter, UK) ,  Sian Ellard, BSc, PhD, FRCPath, OBE (Consultant Clinical Molecular Geneticist, Royal Devon and Exeter Hospital<br>Professor of Human Molecular Genetics, Peninsula Medical School, Exeter, UK) ,  Ruth Cleaver, Mbchb BSC MRCP (Clinical Genetics<br>Royal Devon and Exeter NHS Foundation Trust<br>Exeter, United Kingdom)
Publisher:   Elsevier Health Sciences
Edition:   16th edition
ISBN:  

9780702079665


Pages:   448
Publication Date:   13 February 2021
Replaced By:   9780702067433
Format:   Paperback
Availability:   In stock   Availability explained
We have confirmation that this item is in stock with the supplier. It will be ordered in for you and dispatched immediately.

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Emery's Elements of Medical Genetics and Genomics


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Overview

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. Turnpenny and Sian Ellard, as well as new editor Ruth Cleaver. Enhanced eBook version included with purchase. Your enhanced eBook allows you to access all of the text, figures, and references from the book on a variety of devices.

Full Product Details

Author:   Peter D Turnpenny, BSc MB ChB DRCOG DCH FRCP FRCPCH FRCPath FHEA (Consultant Clinical Geneticist, Royal Devon and Exeter Hospital<br>Senior Clinical Lecturer, Peninsula Medical School, Exeter, UK) ,  Sian Ellard, BSc, PhD, FRCPath, OBE (Consultant Clinical Molecular Geneticist, Royal Devon and Exeter Hospital<br>Professor of Human Molecular Genetics, Peninsula Medical School, Exeter, UK) ,  Ruth Cleaver, Mbchb BSC MRCP (Clinical Genetics<br>Royal Devon and Exeter NHS Foundation Trust<br>Exeter, United Kingdom)
Publisher:   Elsevier Health Sciences
Imprint:   Elsevier Health Sciences
Edition:   16th edition
Weight:   1.240kg
ISBN:  

9780702079665


ISBN 10:   0702079669
Pages:   448
Publication Date:   13 February 2021
Audience:   College/higher education ,  Tertiary & Higher Education
Replaced By:   9780702067433
Format:   Paperback
Publisher's Status:   Active
Availability:   In stock   Availability explained
We have confirmation that this item is in stock with the supplier. It will be ordered in for you and dispatched immediately.

Table of Contents

1 The History and Impact of Genetics in Medicine Section A: The Scientific Basis of Human Genetics 2 The Cellular and Molecular Basis of Inheritance 3 Chromosomes and Cell Division 4 Finding the Cause of Monogenic Disorders by Identifying Disease Genes 5 Laboratory Techniques for Diagnosis of Monogenic Disorders 6 Patterns of Inheritance 7 Population and Mathematical Genetics 8 Risk Calculation 9 Developmental Genetics Section B: Genetics in Medicine and Genomic Medicine 10 Common Disease, Polygenic and Multifactorial Genetics 11 Screening for Genetic Disease 12 Haemoglobin and the Haemoglobinopathies 13 Immunogenetics 14 The Genetics of Cancer. . .and Cancer Genetics 15 Pharmacogenomics, Precision Medicine and the Treatment of Genetic Disease Section C: Clinical Genetics, Counselling and Ethics 16 Congenital Abnormalities, Dysmorphic Syndromes and Intellectual Disability 17 Chromosome Disorders 18 Inborn Errors of Metabolism 19 Mainstream Monogenic Disorders 20 Prenatal Testing and Reproductive Genetics 21 Genetic Counselling 22 Ethical and Legal Issues in Medical Genetics

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