New Clinical Genetics

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New Clinical Genetics, fourth edition

New Clinical Genetics, fourth edition
Author :
Publisher : Scion Publishing Ltd
Total Pages : 470
Release :
ISBN-10 : 9781911510741
ISBN-13 : 1911510746
Rating : 4/5 (746 Downloads)

Book Synopsis New Clinical Genetics, fourth edition by : Andrew Read

Download or read book New Clinical Genetics, fourth edition written by Andrew Read and published by Scion Publishing Ltd. This book was released on 2020-10-23 with total page 470 pages. Available in PDF, EPUB and Kindle. Book excerpt: 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


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