Emery s Elements of Medical Genetics

Author: Peter D Turnpenny
Publisher: Elsevier Health Sciences
ISBN: 0702066893
Format: PDF, ePub
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Everything a student needs to know about medical genetics is here in the 15th edition of this award-winning textbook. Thoroughly updated and revised throughout to map a fast-moving area, the 15th edition continues Emery’s enviable reputation for successfully balancing up-to-dateness in a rapidly developing field with a strong basis in practical clinical genetics for medical students. With MCQs and Case-Based Review Questions, end of chapter summaries, it is the essential tool for this complex but foundational topic for all medical undergraduates, as well as postgraduates seeking to improve their understanding and knowledge. Divided into three restructured sections to make the book easier to use for a variety of readers: Scientific Basis of Human Genetics; Genetics in Medicine and Genomic Medicine; Clinical Genetics, Counselling and Ethics •Interactive self-assessment questions •Case-based questions •Online hyperlinks to important genetics websites and clinical databases. •Update of clinical figures to include more full-colour images •An extensive glossary of terms •Full colour art to visualise the appearance of genetic disorders and assist with the understanding of complex genetic structures •Explore the social, ethical and counselling issues surrounding the study and treatment of genetic disorders. •Elements boxes at the end of each chapter summarizing the basics at a glance.

Elements of Medical Genetics

Author: Alan E. H. Emery
Publisher:
ISBN: 9780443045240
Format: PDF, Docs
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Updated and revised, with new illustrations, diagrams and clinical photographs. There is also new information on molecular biology and molecular genetics and it is in a larger format and colour has been added for the first time. It is a text for students in preclinical as well as clinical years.

Medical Genetics

Author: Lynn B. Jorde
Publisher: Elsevier Health Sciences
ISBN: 0323188354
Format: PDF, ePub, Mobi
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Popular for its highly visual, clinical approach, Medical Genetics delivers an accessible yet thorough understanding of this active and fast-changing field. Key updates in this new edition cover the latest developments which are integrated with clinical practice to emphasize the central principles and how they apply to practice. Photographs, illustrations, and tables, along with boxes containing patient/family vignettes demonstrate clinical relevance and enhance visual impact of the material for easier and more effective learning and retention. Includes access to the complete text and images online at studentconsult.com along with 200 additional USMLE-style questions for self-assessment. Mini-summaries, study questions, suggested reading, and a detailed glossary supplement and reinforce what you learn from the text. More than 230 photographs, illustrations, and tables, along with patient/family vignettes clarify difficult concepts and demonstrate clinical significance. Clinical Commentary Boxes help demonstrate how the hard science of genetics has real applications to everyday patient problems and prepare you for problem-based integrated courses. The latest knowledge and research on gene identification, cancer genetics, gene testing and gene therapy, common disorders, ethical and social issues, and much more so you can keep up with current developments in genetics. Student Consult eBook version included with purchase. This enhanced eBook experience allows access to 200 additional USMLE questions, as well as new materials (outlined above) designed to produce a more rounded learning experience.

Oxford Handbook of Genetics

Author: Guy Bradley-Smith
Publisher: Oxford University Press
ISBN: 0199545367
Format: PDF, ePub
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Genetics is a rapidly changing field, making it difficult for Primary Care practitioners to keep up to date. This book is a collaboration between 2 consultant geneticists, and 2 experienced GPs. This small book provides accessible information, including explanatory diagrams and family trees, about both specific genetic diseases and the possible genetic components of major diseases, such as heart disease and diabetes, for the primary health care team. It aims tohelp practitioners to know why, when and where they should refer patients or affected families to get the best advice about, or surveillance of, genetic disease. It also contains information about the genetic testing which may be offered in secondary care. Each chapter also contains a list ofresources which might be of further use to the practitioner or their patient. There are chapters on cancer, as well as antenatal screening, and specific problems that may arise from such screening.

Oxford Desk Reference Clinical Genetics and Genomics

Author: Helen V. Firth
Publisher: Oxford University Press
ISBN: 0192519832
Format: PDF, Mobi
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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. 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.

Secondary Data Sources for Public Health

Author: Sarah Boslaugh
Publisher: Cambridge University Press
ISBN: 9781139464475
Format: PDF, Kindle
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Secondary data play an increasingly important role in epidemiology and public health research and practice; examples of secondary data sources include national surveys such as the BRFSS and NHIS, claims data for the Medicare and Medicaid systems, and public vital statistics records. Although a wealth of secondary data is available, it is not always easy to locate and access appropriate data to address a research or policy question. This practical guide circumvents these difficulties by providing an introduction to secondary data and issues specific to its management and analysis, followed by an enumeration of major sources of secondary data in the United States. Entries for each data source include the principal focus of the data, years for which it is available, history and methodology of the data collection process, and information about how to access the data and supporting materials, including relevant details about file structure and format.

History of Human Genetics

Author: Heike I. Petermann
Publisher: Springer
ISBN: 331951783X
Format: PDF, ePub
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Written by 30 authors from all over the world, this book provides a unique overview of exciting discoveries and surprising developments in human genetics over the last 50 years. The individual contributions, based on seven international workshops on the history of human genetics, cover a diverse range of topics, including the early years of the discipline, gene mapping and diagnostics. Further, they discuss the status quo of human genetics in different countries and highlight the value of genetic counseling as an important subfield of medical genetics.

Essential Neuroscience

Author: Allan Siegel
Publisher: Lippincott Williams & Wilkins
ISBN: 0781783836
Format: PDF, Kindle
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The Second Edition covers fundamental neuroscience topics, integrating essential information with clinical and physiological considerations, providing students with multiple opportunities for review and self-testing, and presenting the latest relevant developments in neuroscience.