Since its introduction in 2012, cell-free (cf) DNA based Non-Invasive Prenatal Testing (NIPT) has been employed to test for fetal chromosome abnormalities, and gene mutations that lead to a variety of genetic conditions, by millions of pregnant women...Lasīt vairāk
Since its introduction in 2012, cell-free (cf) DNA based Non-Invasive Prenatal Testing (NIPT) has been employed to test for fetal chromosome abnormalities, and gene mutations that lead to a variety of genetic conditions, by millions of pregnant women...Lasīt vairāk
Get a quick, expert overview of the many key facets of pediatric cancer genetics with this concise, practical resource by Dr. Nathaniel H. Robin and Meagan Farmer, MS, CGC, MBA. Ideal for pediatric oncologists and all providers who care for children,...Lasīt vairāk
National Academies of Sciences, Engineering, and Medicine, Health and Medicine Division, Board on Health Care Services, Board on the Health of Select Populations, Committee on the Evidence Base for Genetic Testing
(Izdošanas datums: 21-Mar-2017, PDF+DRM, Izdevniecība: National Academies Press, ISBN-13: 9780309453301)
Advances in genetics and genomics are transforming medical practice, resulting in a dramatic growth of genetic testing in the health care system. The rapid development of new technologies, however, has also brought challenges, including the need for...Lasīt vairāk
National Academies of Sciences, Engineering, and Medicine, Health and Medicine Division, Board on Health Care Services, Board on the Health of Select Populations, Committee on the Evidence Base for Genetic Testing
(Izdošanas datums: 21-Mar-2017, EPUB+DRM, Izdevniecība: National Academies Press, ISBN-13: 9780309453325)
Advances in genetics and genomics are transforming medical practice, resulting in a dramatic growth of genetic testing in the health care system. The rapid development of new technologies, however, has also brought challenges, including the need for...Lasīt vairāk
An essential manual for the future of genetic counselingGenetic counselors possess the important set of skills necessary to face the unique challenges encountered within the laboratory. As the primary liaisons between genetic technologies and patient...Lasīt vairāk
An essential manual for the future of genetic counselingGenetic counselors possess the important set of skills necessary to face the unique challenges encountered within the laboratory. As the primary liaisons between genetic technologies and patient...Lasīt vairāk
Incorporate genomics into every applicable area of your clinical practice with this complete how-to guideA Doodys Core Title for 2024 & 2021!Precision Medicine: A Guide to Genomics in Clinical Practice is a comprehensive, yet succinct overview o...Lasīt vairāk
Incorporate genomics into every applicable area of your clinical practice with this complete how-to guideA Doodys Core Title for 2024 & 2021!Precision Medicine: A Guide to Genomics in Clinical Practice is a comprehensive, yet succinct overview o...Lasīt vairāk
Alcohol, Drugs, Genes and the Clinical Laboratory provides an overview and quick reference to genetic relationships and clinical laboratory information related to the serious public health issue of alcohol and drug abuse. Written in a clear and conci...Lasīt vairāk
Alcohol, Drugs, Genes and the Clinical Laboratory provides an overview and quick reference to genetic relationships and clinical laboratory information related to the serious public health issue of alcohol and drug abuse. Written in a clear and conci...Lasīt vairāk
The clinical features of periodontal diseases in children and adolescents differ from those in adults. Periodontitis is extremely rare in children, except those complicated with certain kinds of systemic diseases, whereas gingivitis is commonly encou...Lasīt vairāk
This book looks at genetic screening of newborns and the ethical principles that guide this practice. The majority of babies born in the U.S. each year undergo screening soon after birth to identify genetic defects that could cause serious illness if...Lasīt vairāk
This book presents current research from across the globe in the study of genetic diagnoses. Topics discussed include the genetic risk factors between thyroid function and preeclampsia; the molecular diagnosis of thalessemia and spinocerebelar ataxia...Lasīt vairāk
This book provides an overview of the nonclinical testing strategies that are used to asses and de-risk the genotoxicity and carcinogenicity properties of human pharmaceuticals. It includes a review of relevant ICH guidelines, numerous case studies w...Lasīt vairāk
Sērija : Studies for the Society for the Social History of Medicine
(Izdošanas datums: 06-Oct-2015, PDF+DRM, Izdevniecība: Taylor & Francis Ltd, ISBN-13: 9781317319030)
This collection of essays looks at issues of health and citizenship in Europe across two centuries. Contributors examine the extent to which the state can interfere with the private lives of its citizens, the role of individual responsibility and if...Lasīt vairāk
Sērija : Studies for the Society for the Social History of Medicine
(Izdošanas datums: 06-Oct-2015, EPUB+DRM, Izdevniecība: Taylor & Francis Ltd, ISBN-13: 9781317319023)
This collection of essays looks at issues of health and citizenship in Europe across two centuries. Contributors examine the extent to which the state can interfere with the private lives of its citizens, the role of individual responsibility and if...Lasīt vairāk
This important book proposes revising the current informed consent protocol for predictive genetic testing to reflect the trend toward patient-centered medicine. Emphasizing the predictive aspect of testing, the author analyzes the state of informed...Lasīt vairāk
Knowledge of the genetic basis of human diseases is growing rapidly, with important implications for pre-conceptional, prenatal, and predictive testing. While new genetic testing offers better insight into the causes of and susceptibility for heritab...Lasīt vairāk
Knowledge of the genetic basis of human diseases is growing rapidly, with important implications for pre-conceptional, prenatal, and predictive testing. While new genetic testing offers better insight into the causes of and susceptibility for heritab...Lasīt vairāk
AimsTo some, the field of neurogenetics appears perplexing and indecipherable. In this volume, we will address this issue by providing clinicians with a framework for dealing with these disorders. This book is not intended to be an in-depth, comprehe...Lasīt vairāk
AimsTo some, the field of neurogenetics appears perplexing and indecipherable. In this volume, we will address this issue by providing clinicians with a framework for dealing with these disorders. This book is not intended to be an in-depth, comprehe...Lasīt vairāk
Connecting an abnormal physical exam to a possible genetic condition is a daunting and inexact task for any physician, be they a primary care provider, non-geneticist specialist, or fellowship-trained geneticist. Comprising 31 clinical protocols from...Lasīt vairāk
Toxicogenomics-Based Cellular Models is a unique and valuable reference for all academic and professional researchers employing toxicogenomic methods with respect to animal testing for chemical safety. This resource offers cutting-edge information on...Lasīt vairāk
Toxicogenomics-Based Cellular Models is a unique and valuable reference for all academic and professional researchers employing toxicogenomic methods with respect to animal testing for chemical safety. This resource offers cutting-edge information on...Lasīt vairāk
