New Clinical Genetics
New Clinical Genetics by Andrew P. Read, published by Scion in 2015, is the third edition of this comprehensive text, spanning 448 pages in English. This edition reflects significant advancements in the understanding, diagnosis, and treatment of genetic diseases, incorporating updates based on current literature and the latest technological progress, particularly in whole-genome sequencing.
Readers will find a unique case-based approach that enhances the learning experience, making it suitable for medical students and professionals in genetics. The book covers essential topics such as next-generation sequencing, noninvasive prenatal diagnosis, and epigenetics, while also providing detailed discussions on conditions like mosaicism and RASopathies. This resource serves as both a textbook and a guide for genetic counselors, physician assistants, and clinical geneticists, maintaining its relevance in the evolving field of medical genetics.
Official synopsis Publisher
Instructors’ comments on new, 3rd, edition:
“I LOVED the book. I’ve never seen anything like it, and I’ve reviewed a lot of genetics texts. The way that cases are presented throughout is extremely novel.”
“I am greatly pleased with the revisions. In my opinion, there is an increased clarity in the text (which will serve students well), and many welcomed updates based on current literature. Good job!”
“I LIKE IT A LOT!!”
“The book looks good and we will certainly be recommending it for our medical genetics course this autumn.”
“This is a fantastic book that I enjoy so much teaching from.”
“I have been reviewing the book. I think it is a great teaching tool since you can follow a case from beginning to end.”
“I have used this book every year since the first edition was published and it is a perfect fit for my human genetics course. I will definitely continue to use it.”
“It’s great. I will recommend the book as a main text for the medical student class.”
In the few years since the previous edition technical progress, especially the widespread use of whole-genome technologies, has brought many advances in the understanding, diagnosis and treatment of genetic disease. As a result, most chapters have been substantially rewritten and updated to reflect this. The unique structure and format remains the same, but significant new material has been added to cover:
-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
-noninvasive prenatal diagnosis by next-generation sequencing of free fetal DNA in the maternal circulation
-a new integrated treatment of epigenetics
-mosaicism, ‘RASopathies’ and disorders of the spliceosome are described in new Disease boxes
-dysmorphology in more detail New Clinical Genetics continues to offer the most innovative case-based approach to modern genetics.
It is used worldwide as a textbook for medical students, but also as an essential guide to the field for genetic counselors, physician assistants, and clinical and nurse geneticists.
Reviews of earlier editions:
“This book provides a wonderful case-based learning environment. There are also self-assessment questions. Students are not given model answers but are provided with guidance on how to work out the correct answers for themselves. Excellent!” Human Genetics
“This book is a very valuable tool that will be used by future geneticists all over Europe and beyond, both as a teaching material and as a source of excellent knowledge.” European Journal of HumanGenetics
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