
Introduction to Risk Calculation in Genetic Counseling
Ian Young(Author)
Oxford University Press
2nd Edition
Published on 9. September 1999
Book
Paperback/Softback
228 pages
978-0-19-262962-3 (ISBN)
Shipment within 15-20 days
Description
Genetic counselling is widely accepted as an integral part of the management of every patient with an inherited disorder, and the rapid developments in human and medical genetics have reinforced the importance of competency in risk calculation. Fully updated since the first edition (1991) this book provides a simple introduction for risk calculation for genetics counselling,, describing how risks can easily be estimated or calculated for most counselling situations. Easy-to-use, with worked examples, this book covers all patterns of inheritance. In this second edition, Introduction to Risk Calculation for Genetic Counselling now includes a chapter on cancer genetics, and there are also new sections on anticipation, gonadal mosaicism, the potential use of susceptibility loci, three-way chromosome translocations and meiotic drive.
Reviews of the first edition: 'This is a good book' American Journal of Human Genetics 'I would recommend this book to any clinicians involved in aspects of genetic counselling' Genetical Research Introduction to Risk calculation for Genetic Counselling.. 'is simple, clear and accurate.' 'There is no doubt that this will be a popular book.' Journal of Medical Genetics 'Introduction to risk calculation in genetic counselling more than fulfills its aim to be a "user-friendly introduction to risk calculation.... For those involved in the delivery of genetic counselling services." It is clear in style, with worked example, and all within 150 pages.' BMJ 'This new text is to be welcomed as it is readily accessible to the majority of clinicians and is, in essence, a book that should be in the "working bookshelf"!' Neuromuscular Disorders
Reviews of the first edition: 'This is a good book' American Journal of Human Genetics 'I would recommend this book to any clinicians involved in aspects of genetic counselling' Genetical Research Introduction to Risk calculation for Genetic Counselling.. 'is simple, clear and accurate.' 'There is no doubt that this will be a popular book.' Journal of Medical Genetics 'Introduction to risk calculation in genetic counselling more than fulfills its aim to be a "user-friendly introduction to risk calculation.... For those involved in the delivery of genetic counselling services." It is clear in style, with worked example, and all within 150 pages.' BMJ 'This new text is to be welcomed as it is readily accessible to the majority of clinicians and is, in essence, a book that should be in the "working bookshelf"!' Neuromuscular Disorders
Reviews / Votes
I would recommend this book to any clinicians involved in aspects of genetic counselling * Genetical Research * Introduction to Risk Calculation in Genetic Counselling more than fulfils its aim to be a "user friendly introduction to risk calculation... for those involved in deliver of genetic counselling services." It is clear in style, with worked examples, and all within 150 pages * BMJ, vol 307 * ...this new text is to be welcomed as it is readily accessible to the majority of clinicians and is, in essence, a book that should be on the "working bookshelf"! * Neuromuscular Disorders *More details
Edition
2nd Revised edition
Language
English
Place of publication
Oxford
United Kingdom
Target group
College/higher education
Professional and scholarly
Edition type
Revised edition
Illustrations
figures and tables
Dimensions
Height: 234 mm
Width: 156 mm
Thickness: 13 mm
Weight
360 gr
ISBN-13
978-0-19-262962-3 (9780192629623)
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
New editions

Book
10/2006
3rd Edition
Oxford University Press Inc
€93.30
Shipment within 15-20 days
Previous edition

Book
04/1991
Oxford University Press
€68.09
Article exhausted; check for reprint
Person
Author
Consultant and Professor of Paediatric GeneticsConsultant and Professor of Paediatric Genetics, Nottingham City Hospital