Mutation detection is increasingly undertaken in a wide spectrum of research areas: in medicine it is fundamental in isolating disease genes and diagnosis, and is especially important in cancer research; in biology, commercially important genes can be identified by the mutations they contain. But mutation detection is time-consuming and expensive. This volume offers tried and tested protocols for a range of detection methods, from the labs of the leading researchers in the field.
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very comprehensive book ... The text is well referenced and includes useful examples in which the techniques have been employed successfully. The guidance given on the choice of technique and strategies to be adopted is very helpful. The layout of the book makes it a very clear and user friendly reference text. It is up to date, with brief descriptions of emerging technqiues. (Ann Curtis, TIG November 1997 Vol. 13 No. 11)
an elegant and balanced account of mutation detection, setting the subject in a truly academic format ... Both the historical developments and basic principles are brought together in a clear and very thorough way, and the presentation should empower the reader to 'go away and think for himself' ... The detail given is considerable, and the author has structured the chaos of developments into as comprehensive overview ... this is an outstanding little book (Ian Day, UCLMS, Epidemiology & Infection, Vol. 119, 1997)
Cotton's book is an elegant and balanced account of mutation detection, setting the subject in a truly academic format. Both the historical developments and basic principles are brought together in a clear and very thorough way, and the presentation should empower the reader to 'go away and think for himself'. The detail given is considerable, and the author has structured the chaos of developments into a comprehensive overview ... this is an outstanding little book. (I. Day, UCLMS, Annals of Human Genetics, Vol. 61, 1997)
With its readable format that summarizes and yet still offers practical directions, this book provides an excellent window into the complex array of new molecular diagnostics for human diseases. The introduction is clearly written. ... this book will not be redundant in the near future ... this book contains materials that would normally be scattered among different experts and diverse journals, but which are handily addressed in one slim readable volume. (Linda Surh, Annals of the Royal College of Phsycians and Surgeons of Canada, vol. 31, no. 2, March 1998)
'...This book is written by Richard Cotton, editor of Human Mutation, one of the fastest growing olecular biolgoy journals, so his credentials are well proven...the introductory chapter is short and concise, and also packed with useful tables...The next five chapters are a concise and in depth account of the main methods used, covering: sequencing methods, scanning methods, diagnostic methods, associated techniques and strategies for mutation detection...MD or PhD students undertaking research involving molecular genetic techniques will find this book is an excellent starter.' (Patrick J Morrison, Ulster Medical Society)
'There can be few authors better placed to write such a book than Professor Cotton...This volume is a comprehensive source for references and background on the most widely used (and a few of more esoteric) mutation detection methods and is a useful introdution to the topic.' (GR Taylor, St James's University Hospital)
R. G. H. Cotton is at Mutation Research Centre, Victoria. E. Edkins is at Joint Women's and Children's Hospital, Perth.
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