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- Elsevier Science 2014; US$ 150.00
Clinical Genomics provides an overview of the various next-generation sequencing (NGS) technologies that are currently used in clinical diagnostic laboratories. It presents key bioinformatic challenges and the solutions that must be addressed by clinical genomicists and genomic pathologists, such as specific pipelines for identification of the full... more...
- Taylor and Francis 2009; US$ 54.95
Carrier testing of adults provides information about the risk of passing a genetic mutation to your children, leading to reproductive (and some say, eugenic) decisions. Excessive carrier screening may have adverse effects, but it can also prevent suffering and open up new reproductive options. Raz's study focuses on the interplay of community genetics... more...
- Humana Press 2007; US$ 189.00
Ultimately, the quality of the tools available for genetic analysis and experimental disease models will be assessed on the basis of whether they provide new information that generates novel treatments for human disease. In addition, the time frame in which genetic discoveries impact clinical practice is also an important dimension of how society assesses... more...
- Springer Berlin Heidelberg 2009; US$ 259.00
This book is designed to serve the radiologist as a simple visual guide that illustrates the typical diagnostic radiological features of the most common congenital diseases and syndromes. It includes supplementary high-quality digital medical illustrations. more...
- World Scientific Publishing Company 2007; US$ 227.00
The sequencing of the human genome has brought human genetics into a new era of study resulting in the generation of an explosive amount of information. Application of genomic, proteomic, and bioinformatics technologies to the study of human genetics has made it possible for human genetic diseases to be studied on an unprecedented scale, both in silico... more...
- University of California Press 2008; US$ 15.95
The genetic revolution has provided incredibly valuable information about our DNA, information that can be used to benefit and inform?but also to judge, discriminate, and abuse. An essential reference for living in today's world, this book gives the background information critical to understanding how genetics is now affecting our everyday lives. Written... more...
- Springer Fachmedien Wiesbaden 2014; US$ 49.99
?Mit Hilfe prädiktiv-gendiagnostischer Untersuchungsverfahren gelingt die Identifizierung genetischer Risikofaktoren weit vor Sichtbarwerdung erster Erkrankungssymptome. Am Beispiel der prädiktiven Brustkrebsdiagnostik begründet Ariane Schroeder das Recht auf Nichtwissen aus Sicht einer aufgeklärten Patientenautonomie positiv und profiliert es als... more...
- McFarland & Company, Inc., Publishers 2007; US$ 35.00
The number of people suffering from Multiple Chemical Sensitivity (MCS) is greater than the number suffering from AIDS, yet the general public and the medical community know very little about the disease. More and more people are disabled daily, despite the fact that the condition does not have to occur. In Part One of this work, experts review the... more...
- Elsevier Science 2014; US$ 210.00
This well-established international series examines major areas of basic and clinical research within neuroscience, as well as emerging and promising subfields. This volume concentrates on Epigenetics This book looks at Epigeneticsin the light of the newest scholarly discoveries and insights. more...
- Elsevier Science 2015; US$ 125.00
Epigenetics and Dermatology explores the role of epigenetics in the pathogenesis of autoimmune-related skin diseases and skin cancer. Leading contributors cover common and uncommon skin conditions in which extensive epigenetic research has been done. They explain how environmental exposures (chemicals, drugs, sunlight, diet, stress, smoking, infection,... more...