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Oxford Desk Reference: Clinical Genetics and Genomics
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Oxford Desk Reference: Clinical Genetics and Genomics

2 Revised edition

Book Details

Format Hardback or Cased Book
ISBN-10 0199557500
ISBN-13 9780199557509
Edition 2 Revised edition
Publisher Oxford University Press
Imprint Oxford University Press
Country of Manufacture GB
Country of Publication GB
Publication Date Sep 7th, 2017
Print length 944 Pages
Weight 1,924 grams
Dimensions 25.50 x 17.80 x 5.10 cms
Product Classification: Medical genetics
Ksh 25,150.00
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The new edition of this classic text provides a practical, easy-to-use guide to clinical consultation in genetics, covering the process of diagnosis, investigation, management, and counselling for patients. All genetic conditions are covered as well as referral categories for a clinical genetic opinion.
A popular and easy-to-use guide, this book is a must-have tool for clinical consultations in genetics and genomic medicine.Ideal for quick reference during practice, it covers the process of diagnosis, investigation, management, and counselling for patients. With a strong evidence base and international guidelines, it puts reliable and trustworthy guidance at your fingertips. Designed for use as a first-line guide, the A to Z format ensures it''s accessible, and the simple layout makes it easy to assimilate information. Highly illustrated, the book also contains up-to-date glossaries of terms used in genetics and dysmorphology providing quick reference for key concepts. The second edition is an eagerly anticipated update of the gold standard in the specialty. It covers new developments in the field, particularly the advent of genome-wide sequencing and major updates in cancer. Fifteen new topics have been added, including Sudden cardiac death, Neonatal screening, and Ciliopathies. The authors have used their experience to devise a practical clinical approach to many common genetic referrals, both outpatient and ward based. The most common Mendelian disorders, chromosomal disorders, congenital anomalies and syndromes are all covered, and where available diagnostic criteria are included. In addition there are chapters on familial cancer and pregnancy-related topics such as fetal anomalies, teratogens, prenatal and pre-implantation diagnosis and non-invasive prenatal testing. The book also provides information on the less common situations where management is particularly complex. Both practical and pertinent, Oxford Desk Reference: Clinical Genetics and Genomics is the companion you need by your side during clinical consultations.

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