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Human genetics --- Medical genetics --- Genetics, Medical --- Genetic Diseases, Inborn --- Génétique médicale --- Periodicals --- Périodiques --- Genetics, Medical. --- Genetic Diseases, Inborn. --- Medical genetics. --- Genetics & Genomics. --- Clinical genetics --- Diseases --- Heredity of disease --- Genetic Diseases --- Genetic Disorders --- Hereditary Disease --- Inborn Genetic Diseases --- Single-Gene Defects --- Hereditary Diseases --- Defect, Single-Gene --- Defects, Single-Gene --- Disease, Genetic --- Disease, Hereditary --- Disease, Inborn Genetic --- Diseases, Genetic --- Diseases, Hereditary --- Diseases, Inborn Genetic --- Disorder, Genetic --- Disorders, Genetic --- Genetic Disease --- Genetic Disease, Inborn --- Genetic Disorder --- Inborn Genetic Disease --- Single Gene Defects --- Single-Gene Defect --- Human Genetics --- Medical Genetics --- Genetics, Human --- Genetic aspects --- medical genetics --- Medical sciences --- Pathology --- Genetic disorders --- Anthropology, Physical --- Chromosome Disorders --- Sex Chromosome Disorders --- Molecular Medicine --- Genetics

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This is one of the few medical genetics texts on a 2-year revision cycle. It provides up-to-date information that can be read, retained, and applied with ease! The 3rd Edition covers pharmacogenomics: the societal implications of technologies: the Human Genome Project; cloning, genetic enhancement, and embryonic stem cell research: new tumor suppressor genes and oncogenes and more. Mini-summaries, study questions, suggested readings, and a detailed glossary facilitates review of the material. Clinical relevance is demonstrated in over 230 photographs, illustrations, and tables as well as boxes containing patient/family vignettes, coverage of ethical, legal, and social issues and clinical commentary on important genetic diseases. A companion web site offers continuing updates and a wealth of additional features.

Human genetics --- moleculaire biologie --- Molecular biology --- medische genetica --- Genetic Diseases, Inborn --- Genetics, Medical. --- Medical Genetics --- Anthropology, Physical --- Chromosome Disorders --- Sex Chromosome Disorders --- Molecular Medicine --- genetics. --- Medical genetics. --- Hereditary Diseases --- stamcellen --- klonen --- tumoren --- Genetics, Medical --- genetics --- Hereditary Diseases - genetics.

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Genomics --- Human genetics --- Gene mapping --- Genomes --- Genetique humaine --- Cartes chromosomiques --- Genome --- Chromosome Mapping --- Genetics, Medical --- Genetics --- Genome Mapping --- Gene Mapping --- Linkage Mapping --- Chromosome Mappings --- Gene Mappings --- Genome Mappings --- Linkage Mappings --- Mapping, Chromosome --- Mapping, Gene --- Mapping, Genome --- Mapping, Linkage --- Mappings, Chromosome --- Mappings, Gene --- Mappings, Genome --- Mappings, Linkage --- Human Genetics --- Medical Genetics --- Genetics, Human --- Cytogenetics --- Genetic Markers --- Cytogenetic Analysis --- Gene Order --- Synteny --- Anthropology, Physical --- Chromosome Disorders --- Sex Chromosome Disorders --- Genetic Diseases, Inborn --- Molecular Medicine --- Genes --- Proteome --- Genome. --- Genetics, Medical. --- Chromosome Mapping.

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th This volume contains articles presented at the X International Symposium on Purines and Pyrimidines in Man, held on May 14 19, 2000 in Tel Aviv, Israel. The first symposium in this series took place in Tel Aviv in 1973. Since then, the symposium has been held every three years in different parts of the world, including Europe, USA and Japan. The participants, in this series of symposia, are characterised by a wide interest in the various aspects of purines and pyrimidines in man, which include biochemistry, genetics, pharmacology, physiology, clinics, etc. Presentations in the symposia include clarification of metabolic pathways, characterisation of enzyme structure and kinetics and discoveries of new inborn errors of metabolism and suggestions for new therapeutic approaches for these inborn errors. In addition, development of new purine and pyrimidine derivatives for the treatment of cancer and viral diseases, and many more subjects of mutual interest were brought to the fore. With the development of therapeutic means and of new research tools, we have witnessed changes in the areas of interest. The interest in gout and uric acid urolithiasis has lessened, whereas molecular aspects, the role of purine and pyrimidine substances in neurotransmission and in purinergic signaling appear to gain greater interest. The articles, included in this volume, contain new data pertaining to the various aspects detailed above.

Electronic books. -- local. --- Purines -- Metabolism -- Congresses. --- Purines -- Metabolism -- Disorders -- Congresses. --- Pyrimidines -- Metabolism -- Congresses. --- Pyrimidines -- Metabolism -- Disorders -- Congresses. --- Purines --- Pyrimidines --- Metabolism, Inborn Errors --- Publication Formats --- Metabolic Phenomena --- Heterocyclic Compounds, 1-Ring --- Heterocyclic Compounds, 2-Ring --- Phenomena and Processes --- Publication Characteristics --- Heterocyclic Compounds --- Metabolic Diseases --- Genetic Diseases, Inborn --- Nutritional and Metabolic Diseases --- Chemicals and Drugs --- Congenital, Hereditary, and Neonatal Diseases and Abnormalities --- Diseases --- Purine-Pyrimidine Metabolism, Inborn Errors --- Congresses --- Metabolism --- Disorders --- Life sciences. --- Cancer research. --- Medical biochemistry. --- Biochemistry. --- Life Sciences. --- Biochemistry, general. --- Medical Biochemistry. --- Cancer Research. --- Oncology. --- Cancer research --- Medical biochemistry --- Pathobiochemistry --- Pathological biochemistry --- Biochemistry --- Pathology --- Biological chemistry --- Chemical composition of organisms --- Organisms --- Physiological chemistry --- Biology --- Chemistry --- Medical sciences --- Composition --- Heterocyclic compounds --- Uric acid

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Genetics --- Genetics, Medical --- Genetic Predisposition to Disease --- Genetic Screening --- Genome --- Medical genetics --- Genomics --- Génétique médicale --- Génomique --- Periodicals. --- Périodiques --- Genomes --- Human genome --- Genetics, Medical. --- Genome. --- Genetic Testing. --- Genetic Predisposition to Disease. --- Genomes. --- Human genome. --- Medical genetics. --- Chemistry --- Health Sciences --- Life Sciences --- Biochemistry --- Pathology --- Predisposition, Genetic --- Susceptibility, Genetic --- Genetic Predisposition --- Genetic Susceptibility --- Genetic Predispositions --- Genetic Susceptibilities --- Predispositions, Genetic --- Susceptibilities, Genetic --- Disease Susceptibility --- Predictive Genetic Testing --- Predictive Testing, Genetic --- Testing, Genetic Predisposition --- Genetic Predisposition Testing --- Genetic Predictive Testing --- Genetic Screenings --- Genetic Testing, Predictive --- Predisposition Testing, Genetic --- Screening, Genetic --- Screenings, Genetic --- Testing, Genetic --- Testing, Genetic Predictive --- Testing, Predictive Genetic --- Human Genetics --- Medical Genetics --- Genetics, Human --- genetics --- diagnosis --- Genetic Testing --- Anticipation, Genetic --- Genetic Association Studies --- Gene-Environment Interaction --- Prenatal Diagnosis --- Preimplantation Diagnosis --- Cytogenetic Analysis --- Molecular Diagnostic Techniques --- Databases, Genetic --- Databases, Nucleic Acid --- Genetic Privacy --- Genes --- Proteome --- Anthropology, Physical --- Chromosome Disorders --- Sex Chromosome Disorders --- Genetic Diseases, Inborn --- Molecular Medicine --- Human chromosomes --- Haploidy --- Clinical genetics --- Diseases --- Heredity of disease --- Human genetics --- Medical sciences --- Genetic disorders --- Genetic aspects