
The Oxford Handbook of Genetics provides an essential overview of this complex subject, distilled into an accessible format for primary care practitioners and junior doctors. It can be used as an aide memoire to gain advice on dealing with individual patients during the working day, or as a reference text to be read over time. Combining the expertise of leading geneticists with the knowledge of experienced general practitioners, the handbook covers the genetics core curriculum as defined by the Royal College of General Practitioners. It includes sections on elementary genetics, single gene disorders, and chromosomal problems, as well as information about the multifactorial diseases, such as ischaemic heart disease, with which practitioners are more familiar. There are also comprehensive sections on antenatal issues, and cancers. A comprehensive glossary with explanations of genetic terminology, and an extensive list of resources, make this book suitable for all healthcare professionals regardless of their level of knowledge or experience. Designed to cross the primary-secondary care interface, this unique handbook covers the gap between general health training and genetic specialist training, including specific advice about when, and how, to make a referral to a genetics service. Given the rapid growth in the genetic knowledge base, this book is designed to be both accessible and informative as a substantive educational resource for practitioners.
This handbook addresses the challenge of integrating complex genetic knowledge into the daily practice of primary care physicians and junior doctors. The authors, a team of geneticists and general practitioners, synthesize clinical data and genetic principles to provide a bridge between general health training and specialized genetic services. The text serves as both a quick-reference aide-memoire for patient consultations and a structured educational resource for ongoing professional development.
What You Will Find
Scope Limits
Medical professionals frequently cite this handbook as a reliable, high-utility resource for bridging the gap between primary care and clinical genetics. Experts highlight the text for its ability to distill dense genetic information into actionable advice for busy practitioners.
Page Count:
485
Publication Date:
2009-01-01
ISBN-10:
0191039659
ISBN-13:
9780191039652
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