New Clinical Genetics, fourth edition
A guide to genomic medicine
4th Edition
Published on 23. October 2020
Book
Paperback/Softback
468 pages
978-1-911510-70-3 (ISBN)
Description
New Clinical Genetics continues to offer the most innovative case-based approach to investigation, diagnosis, and management in genomic medicine.
New Clinical Genetics is used worldwide as a textbook for medical students, but also as an essential guide to the field for genetic counselors, physician assistants, clinical and nurse geneticists, and students studying healthcare courses allied to medicine. Readers love the integrated case-based approach which ties the science to real-life clinical scenarios to really aid understanding.
Clinical genetics is a fast-moving field and there have been many advances in the few years since the previous edition was published. This 4th edition has been completely updated and revised to reflect new science, new techniques and new ways of thinking.
Nowhere is this more clear than in the chapter discussing genetics services which is now significantly expanded to reflect the increasing role of genomic medicine and the use of multidisciplinary teams in the management of patients with genetic disorders.
The unique case-based structure and format remains the same, but substantial new material has been added to cover:
polygenic risk scores - now starting to become useful clinical service tools
preimplantation diagnosis
noninvasive prenatal diagnosis
companion diagnostics for prescribed drugs
liquid biopsies in cancer
epigenetics and gene regulation
the widespread use of next-generation sequencing as a routine diagnostic tool
the checking of a patient's whole exome for the cause of their problem
New Clinical Genetics is used worldwide as a textbook for medical students, but also as an essential guide to the field for genetic counselors, physician assistants, clinical and nurse geneticists, and students studying healthcare courses allied to medicine. Readers love the integrated case-based approach which ties the science to real-life clinical scenarios to really aid understanding.
Clinical genetics is a fast-moving field and there have been many advances in the few years since the previous edition was published. This 4th edition has been completely updated and revised to reflect new science, new techniques and new ways of thinking.
Nowhere is this more clear than in the chapter discussing genetics services which is now significantly expanded to reflect the increasing role of genomic medicine and the use of multidisciplinary teams in the management of patients with genetic disorders.
The unique case-based structure and format remains the same, but substantial new material has been added to cover:
polygenic risk scores - now starting to become useful clinical service tools
preimplantation diagnosis
noninvasive prenatal diagnosis
companion diagnostics for prescribed drugs
liquid biopsies in cancer
epigenetics and gene regulation
the widespread use of next-generation sequencing as a routine diagnostic tool
the checking of a patient's whole exome for the cause of their problem
Reviews / Votes
Incredible Book with Great Teaching Capability'This book is incredibly well put together. The author gives both a typical textbook description of material, as well as a case-study based presentation. There are questions at the end of each chapter to help check your understanding. The only thing I don't like is that there are no provided answers to these questions, only basic hints. However, I recognize why the author did this as it provides a better academic challenge to the reader.
I didn't even buy this for a class. I bought this to read for personal enjoyment and have not been disappointed! Especially for how cheap this is (for a textbook) this is a steal!' Amazon reviewer
More details
Edition
4th Revised edition
Language
English
Place of publication
Bloxham
United Kingdom
Target group
College/higher education
Professional and scholarly
Edition type
Revised edition
Dimensions
Height: 269 mm
Width: 210 mm
Thickness: 22 mm
Weight
1224 gr
ISBN-13
978-1-911510-70-3 (9781911510703)
Copyright in bibliographic data and cover images is held by Nielsen Book Services Limited or by the publishers or by their respective licensors: all rights reserved.
Schweitzer Classification
Other editions
Additional editions
E-Book
10/2020
4th Edition
Scion Publishing
€53.99
Available for download
Previous edition
Andrew Read | Dian Donnai
New Clinical Genetics, third edition
Book
06/2015
3rd Edition
Scion Publishing Ltd
€64.63
Article exhausted; check for reprint
Persons
Content
1 What can we learn from a family history?
2 How can a patient's chromosomes be studied?
3 How do genes work?
4 How can a patient's DNA be studied?
5 How can we check a patient's DNA for gene mutations?
6 What do mutations do?
7 Is cancer genetic?
8 How do researchers identify genes for mendelian diseases?
9 Why are some conditions common and others rare?
10 How do our genes affect our metabolism, drug responses and immune system?
11 How are genes regulated?
12 When is screening useful?
13 Should we be testing for genetic susceptibility to common diseases?
14 What clinical services are available for families with genetic disorders?
15 How to use linkage to map a disease gene
Glossary
Index
Disease index
2 How can a patient's chromosomes be studied?
3 How do genes work?
4 How can a patient's DNA be studied?
5 How can we check a patient's DNA for gene mutations?
6 What do mutations do?
7 Is cancer genetic?
8 How do researchers identify genes for mendelian diseases?
9 Why are some conditions common and others rare?
10 How do our genes affect our metabolism, drug responses and immune system?
11 How are genes regulated?
12 When is screening useful?
13 Should we be testing for genetic susceptibility to common diseases?
14 What clinical services are available for families with genetic disorders?
15 How to use linkage to map a disease gene
Glossary
Index
Disease index