Handbook of Clinical Adult Genetics and Genomics Books

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Handbook of Clinical Adult Genetics and Genomics


Handbook of Clinical Adult Genetics and Genomics
  • Author : Shweta Dhar
  • Publisher : Academic Press
  • Release : 2020-04-10
  • ISBN : 9780128173459
  • Language : En, Es, Fr & De
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Handbook of Clinical Adult Genetics and Genomics: A Practice-Based Approach provides a thorough overview of genetic disorders that are commonly encountered in adult populations and supports the full translation of adult genetic and genomic modalities into clinical practice. Expert chapter authors supplement foundational knowledge with case-based strategies for the evaluation and management of genetic disorders in each organ system and specialty area. Topics discussed include employing genetic testing technologies, reporting test results, genetic counseling for adult patients, medical genetics referrals, issues of complex inheritance, gene therapy, and diagnostic and treatment criteria for developmental, cardiovascular, gastrointestinal, neuropsychiatric, pulmonary issues, and much more. Employs clinical case studies to demonstrate how to evaluate, diagnosis and treat adult patients with genetic disorders Offers a practical framework for establishing an adult genetics clinic, addressing infrastructure, billing, counseling, and challenges unique to adult clinical genetics Features chapter contributions from authors at leading adult genetics institutions in the US and abroad

Oxford Desk Reference Clinical Genetics and Genomics


Oxford Desk Reference  Clinical Genetics and Genomics
  • Author : Helen V. Firth
  • Publisher : Oxford University Press
  • Release : 2017
  • ISBN : 9780199557509
  • Language : En, Es, Fr & De
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Preceded by Oxford desk reference. Clinical genetics / Helen V. Firth, Jane A. Hurst, with Judith G. Hall (consulting editor). 2005.

Handbook of Genomics and the Family


Handbook of Genomics and the Family
  • Author : Kenneth P. Tercyak
  • Publisher : Springer Science & Business Media
  • Release : 2010-08-12
  • ISBN : 1441958002
  • Language : En, Es, Fr & De
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This book introduces readers to the study of how genes, singly and in combination with each other and the environment, affect health and behavior. It provides family-focused perspectives relating to genetic counseling and education.

Oxford Handbook of Genetics


Oxford Handbook of Genetics
  • Author : Guy Bradley-Smith
  • Publisher : Oxford University Press
  • Release : 2009-10-29
  • ISBN : 9780199545360
  • Language : En, Es, Fr & De
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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


Oxford Desk Reference
  • Author : Helen V. Firth
  • Publisher : Oxford University Press, USA
  • Release : 2005
  • ISBN : 0192628968
  • Language : En, Es, Fr & De
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Judith G. Hall is a 2011 Fellow of The Royal Society of Canada. The first in a brand new series of easy-to-use guides, this book is set to become the bible for clinical consultation in genetics. It covers the process of diagnosis, investigation, management, and counselling for patients. Most of the topics fit onto a double-page spread ensuring that the book is an accessible, quick reference for the clinic or hospital consultation. Where available, diagnostic criteria for specific conditions are included as well as contact details for support groups. The book is well illustrated and has an up-to-date bibliography and glossaries of terms used in genetics and dysmorphology. The authors have used their experience to devise a practical clinical approach to many common genetic referrals, both out patient and ward based. The most common Mendelian disorders, chromosomal disorders, congenital anomalies and syndromes are all covered. In addition there are chapters on familial cancer and pregnancy-related topics such as foetal anomalies, teratogens, prenatal and pre-implantation diagnosis. The book also provides information on the less common situations, where management is particularly complex, or important genetic concepts are illustrated.