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Human genetics --- Molecular biology --- Medical genetics --- Abnormalities, Human --- Human chromosome abnormalities --- GENETICS, MEDICAL --- Genetic Diseases, Inborn --- Genetic aspects --- prevention and control --- therapy --- Genetics, Medical. --- -Human chromosome abnormalities --- Clinical genetics --- Diseases --- Heredity of disease --- Medical sciences --- Pathology --- Genetic disorders --- Genetics --- Heredity, Human --- Human biology --- Physical anthropology --- Human chromosomes --- Chromosome abnormalities --- Abnormalities --- Anomalies, Congenital --- Birth defects --- Congenital abnormalities --- Congenital anomalies --- Defects, Birth --- Deformities --- Developmental abnormalities --- Human abnormalities --- Malformations, Congenital --- Morphology --- Teratogenesis --- Teratology --- Human Genetics --- Medical Genetics --- Genetics, Human --- Anthropology, Physical --- Chromosome Disorders --- Sex Chromosome Disorders --- Molecular Medicine --- prevention & control. --- therapy. --- Biotechnologie --- Genetische manipulatie --- Biotechnologie. --- Genetische manipulatie. --- Genetics, Medical --- prevention & control --- Abnormalities, Human - Genetic aspects --- Genetic Diseases, Inborn - prevention and control --- Genetic Diseases, Inborn - therapy
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Medicine. --- Internal medicine. --- Médecine interne --- Internal medicine --- Medicine, Internal --- Medicine --- Medical Specialities --- Medical Specialties --- Medical Specialty --- Specialities, Medical --- Specialties, Medical --- Specialty, Medical --- Medical Speciality --- Speciality, Medical --- Médecine interne --- Health Workforce
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Pathology --- Internal Medicine --- Medicine --- Médecine
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Thalassaemia is the most common type of genetic disorder in the human population, and one of the first whose genetic basis was established. Written by Sir David Weatherall, an expert in molecular medicine and the founder of the Institute of Molecular Medicine in Oxford, this tells the story of early reports of the disease, historical accounts, the identification of the disease as having an inherited basis, early work on thalassaemia as a disorder of the synthesis of haemoglobin, and from the 1960s with the rise of molecular biology, the study of the condition at the DNA level. The commonality
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Written by a leader in the field of genomics, this text discusses genomics-based advances in disease susceptibility, diagnosis, prognostication, and prediction of treatment outcomes. A wide range of clinical areas and the applications now afforded by genomic analysis are discussed.
Medical genetics. --- Genomics. --- Genome research --- Genomes --- Molecular genetics --- Clinical genetics --- Diseases --- Heredity of disease --- Human genetics --- Medical sciences --- Pathology --- Genetic disorders --- Research --- Genetic aspects --- Clinical Medicine. --- Genetic Predisposition to Disease. --- Pharmacogenetics.
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Thalassemia --- Thalassemia. --- Genes --- Hemoglobins
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