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Genomics of Rare Diseases: Understanding Disease Genetics Using Genomic Approaches, a new volume in the Translational and Applied;
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Interventions in Psychiatric Nursing Practice, Genomics in Critical Care, Cardiomyopathy and Genetics, Genetics and Chronic Diseases, Genomics and;
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New discoveries in genomics--that is, the study of the entire human genome--are changing how we diagnose and treat diseases. As the trend;
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indicating the role of genetics in common diseases. Epigenetics and non-coding RNA are covered in-depth as are genetic approaches to treatment and;
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Rare Diseases and Orphan Drugs shows that much of what we now know about common diseases has been achieved by studying rare diseases;
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actionable variants as a way of preventing disease, providing diagnoses for patients with rare diseases, and advancing research on genetic;
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The objective of this book is to catalyze the application of genomics to the diagnosis and treatment of oral diseases by comprehensively;
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There are 7,000 rare diseases affecting 6%-8% of the global population. That's 3.5 million people in the UK alone. Yet only 200 rare;
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, adult-onset glaucoma, diabetic retinopathy, keratoconus, and leber congenital amaurosis, among other diseases. Research and clinical specialists;
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Rare Diseases is een boek van Nova Science Publishers;
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Genes are the determiners of human-inherited traits. The study of the human genome provides a way to understand diseases. Genetic tests can;
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A rare disease is any disease that affects a small percentage of the population. Rare diseases can vary in prevalence between populations;
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Neurodevelopmental diseases affect three percent of children and the specific cause is difficult to determine in many cases. Genetic;
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effects on chronic diseases such as neurological and cardio vascular disorders and a number of rare metabolic disorders such as phenylketonuria;
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Drs. Robert Kotloff and Francis McCormack have assembled an expert team of authors on the topic of Rare and Orphan Lung Diseases. Articles;
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This book focuses on predictive, preventative and personalized medicine (PPPM) and how it is related to the healthcare of rare diseases;
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in regulatory review and approval. Makes recommendations to accurately and reliably evaluate rare diseases regulatory submissions. Proposes innovative;
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in regulatory review and approval. Makes recommendations to accurately and reliably evaluate rare diseases regulatory submissions. Proposes innovative;
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interdisciplinary study of genetics and genomics investigates the interrelationship between genotypes and phenotypes, and between genes and diseases. It;
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affected by rare diseases and to encourage therapies for pediatric patients. During this same time period, the Food and Drug Administration (FDA;
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student interested in learning how molecular genetics is now being applied to prevention and treatment of heart diseases, from DNA tests to;
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of Rheumatoid Arthritis; HLA-disease associations in rheumatoid arthritis; Autoinflammatory Syndromes as a Model of Monogenic Diseases; Genomic;
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becoming relevant in the understanding of common diseases. A patient with a suspected genetic disease undergoes a diagnostic evaluation that;
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factors for complex diseases, the genomics of adaptation and speciation, and other active areas of current research. The principles are;
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factors for complex diseases, the genomics of adaptation and speciation, and other active areas of current research. The principles are;
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