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Item #:
267778003
Oxford Desk Reference: Clinical Genetics and Genomics (Oxford Desk Reference Series)
Item #:
267778003
AUD 150
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A popular and easy-to-use guide, this book is a must-have tool for clinical consultations in genetics and genomic medicine.
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What Stands Out
Comprehensive Resource
Offers an extensive overview of clinical genetics and genomics, serving as a vital reference for healthcare professionals to understand complex genetic information and its implications for patient care.
Expert Insights
Contributed by leading experts in the field, providing authoritative insights that ensure readers receive current and relevant information, enhancing their understanding and application in clinical practice.
User-Friendly Format
Designed for easy navigation, with clear headings and concise sections, making it accessible for practitioners, students, and researchers seeking efficient reference material in genetics and genomics.
Product Details
- 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.
| Publisher | OUP Oxford |
| Publication date | 7 Sept. 2017 |
| Edition | 2nd |
| Language | English |
| Print length | 944 pages |
| ISBN-10 | 0199557500 |
| ISBN-13 | 978-0199557509 |
| Item weight | 2 kg |
| Dimensions | 24.89 x 5.08 x 17.27 cm |
| Part of series | Oxford Desk Reference |
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Medical Genetics Editorial Review
The Oxford Desk Reference: Clinical Genetics And Genomics is an essential resource for those in the clinical genetics field. This 2nd edition, published by OUP Oxford, offers a comprehensive overview across 944 pages, making it a deep dive into genomic medicine. The publication date of September 7, 2017, ensures that the content is relatively up-to-date, reflecting the latest advancements in the field. Readers can expect clear, concise information that is easy to understand, which is praised in many reviews. This reference work serves as a vital tool for medical professionals seeking to enhance their knowledge in genetics and genomics.
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Pros
- Comprehensive overview of clinical genetics
- Clear and concise information
- Updated with recent advancements
- Ideal for medical professionals
- Part of a reputable series
Cons
- Weight may be a bit heavy for portability
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AUD 150
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Only 7 items left in stock.
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Features & Benefits
- Highly accessible A to Z format for quick reference.
- Covers diagnosis, management, and counseling in genetics.
- Includes updates on genome-wide sequencing and cancer.
- Fifteen new topics added, including Sudden cardiac death and Ciliopathies.
- Illustrated with glossaries for easy understanding of terms.
- Companion for both outpatient and ward-based genetic referrals.
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