The essays in this collection examine how human heredity was understood between the end of the First World War and the early 1970s. The contributors explore the interaction of science, medicine and society in determining how heredity was viewed acro...Loe edasi...
Hans D. Ochs, C. I. Edward Smith, Jennifer M. Puck
(Ilmumisaeg: 10-Mar-2014, Kirjastus: Oxford University Press Inc, ISBN-13: 9780195389838)
This third edition of Primary Immunodeficiency Diseases provides readers with the historic and scientific background, clinical presentations, immunologic characteristics, and the molecular/genetic underpinnings of this rapidly enlarging class of dis...Loe edasi...
(Ilmumisaeg: 26-May-2011, Kirjastus: Oxford University Press, ISBN-13: 9780199559688)
Containing summaries of inherited cardiovascular disorders with a focus on aetiology, presentation and management, this handbook covers the fundamentals of molecular biology and genetic testing, and the detailed clinical information relevant to pati...Loe edasi...
(Ilmumisaeg: 25-Mar-2011, Kirjastus: Wiley-Blackwell (an imprint of John Wiley & Sons Ltd), ISBN-13: 9781444329926)
Von Willebrand Disease: Basic and Clinical Aspects provides an insight into all aspects of the condition. Since its discovery, von Willebrand disease has been extensively studied and the causative factor deficiency, the understanding of the conditio...Loe edasi...
(Ilmumisaeg: 25-May-2010, Kirjastus: John Wiley & Sons Inc, ISBN-13: 9780470893159)
It is imperative for primary care providers and genetic practitioners to have access to appropriate management guidelines for the diagnosis, genetic counseling, and management of individuals of all ages affected by relatively common genetic syndrome...Loe edasi...
Provides comprehensive coverage of hereditary aspects of tumor diseases. Summarizes molecular aspects, diagnostic as well as therapeutic issues. Discusses the latest aspects in the diagnosis, disease management, and treatment of hereditary tumor dis...Loe edasi...
(Ilmumisaeg: 12-Feb-2004, Kirjastus: Oxford University Press, ISBN-13: 9780198508786)
Lysosomal storage diseases are metabolic disorders that represent a significant group of diseases that occur in early infancy or childhood. This book will be valuable for clinicians and scientists in helping them understand the molecular mechanisms...Loe edasi...
Recent years have seen rapid advances in our understanding of genetic diseases in terms of their molecular origins. The book focuses on DNA mutations which give rise to abnormalities of protein structure and function in genetic disease....Loe edasi...
