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New edition of an authoritative, practical account, incorporating the latest thinking on the biology of the disease and the best practice in its management. The author works in Jamaica, where the sickle cell trait affects 10% of the population, and he is gratified to report on the significant advances that have been made in the six years since the first edition of his text. Annotation copyright by Book News, Inc., Portland, OR
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Disorders of Hemoglobin stands tall as the definitive work on the genetics, pathophysiology, and clinical management of hemoglobinopathies and thalassemia. Drs. Steinberg, Forget, Higgs, and Nagel have gathered the world authorities on the science and clinical management of these disorders and created the authoritative textbook for researchers and clinicians alike.Authors describe the scientific basis of clinical features and provide clinicians with a clear background of disorders they treat and scientists with an essential link between their research and its clinical manifestation. Disorders of Hemoglobin is the only single-source reference on hemoglobinopathies for hematologists, pediatricians, clinical investigators, and geneticists worldwide.
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