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Thompson & Thompson Genetics in Medicine, editia 7
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- Tip coperta:
- Paperback / softback
- Format:
- 276 mm x 216 mm
- Nr. pagini:
- 600
- Nr. ilustratii:
- 0
- Audienta:
Descriere:
Through six editions, Thompson & Thompson's Genetics in Medicine has been a well-established favourite textbook on this fascinating and rapidly evolving field, integrating the classic principles of human genetics with modern molecular genetics and the latest clinical applications. Clearly written and abundantly illustrated, the New 7th Edition retains all of the features that have made its predecessors so popular while also comprehensively detailing all of the new developments and advances in the field.Introduction
1. Chromosomal Basis of Heredity
2. The Human Genome: Structure and Function of Genes and Chromosomes
3. Tools of Human Molecular Genetics
4. Principles of (Clinical) Cytogenetics
5. Clinical Cytogenetics: Disorders of the Autosomes and the Sex Chromosomes
6. Mechanisms of Inheritance part I: Mendelian (or Single-Gene) Patterns
7. Mechanisms of Inheritance part II: Mitochondrial, Imprinted, and Multifactorial Patterns
8. Genetic Variation in Individuals and Populations
9. The Genetic Contribution to Disease: Locating and identifying Disease Genes
10. Principles of Molecular Disease: Lessons from the Hemoglobinopathies
11. The Molecular and Biochemical Basis of Genetic Disease
12. The Treatment of Genetic Disease
13. Developmental Disorders and Birth Defects (Leslie Biesecker)
14. Genetics of Cancer
15. Genetic Counseling and Risk Assessment
16. Molecular Diagnostics
17. Prenatal Diagnosis
18. Genetics and Society
Case Studies
Through six editions, Thompson & Thompson's Genetics in Medicine has been a well-established favourite textbook on this fascinating and rapidly evolving field, integrating the classic principles of human genetics with modern molecular genetics and the latest clinical applications. Clearly written and abundantly illustrated, the New 7th Edition retains all of the features that have made its predecessors so popular while also comprehensively detailing all of the new developments and advances in the field.Introduction
1. Chromosomal Basis of Heredity
2. The Human Genome: Structure and Function of Genes and Chromosomes
3. Tools of Human Molecular Genetics
4. Principles of (Clinical) Cytogenetics
5. Clinical Cytogenetics: Disorders of the Autosomes and the Sex Chromosomes
6. Mechanisms of Inheritance part I: Mendelian (or Single-Gene) Patterns
7. Mechanisms of Inheritance part II: Mitochondrial, Imprinted, and Multifactorial Patterns
8. Genetic Variation in Individuals and Populations
9. The Genetic Contribution to Disease: Locating and identifying Disease Genes
10. Principles of Molecular Disease: Lessons from the Hemoglobinopathies
11. The Molecular and Biochemical Basis of Genetic Disease
12. The Treatment of Genetic Disease
13. Developmental Disorders and Birth Defects (Leslie Biesecker)
14. Genetics of Cancer
15. Genetic Counseling and Risk Assessment
16. Molecular Diagnostics
17. Prenatal Diagnosis
18. Genetics and Society
Case Studies
Recomandata pentru:
05
05
Despre autori:
By (author): Huntington F. Willard, President and Director, The Research Institute of University Hospitals of Cleveland, Henry Wilson Payne Professor and Chairman, Department of Genetics, Case Western Reserve University School of Medicine; Director, Center for Human Genetics, University Hospitals of Cleveland, Cleveland, OH;
By (author): Roderick R. McInnes, Scientific Director, Institute of Genetics, Canadian Institutes of Health Research, Anne and Max Tanenbaum Chair in Molecular Medicine; Professor of Pediatrics and Molecular and Medical Genetics, University of Toronto and The Hospital for Sick Children, Toronto, Canada;
By (author): Robert Nussbaum, Chief, Genetic Diseases Research Branch; Acting Chief, Inherited Disease Research Branch, National Human Genome Research Institute; Executive Faculty, Johns Hopkins/NHGRI Joint Genetic Counseling Graduate program, National Institutes of Health
By (author): Huntington F. Willard, President and Director, The Research Institute of University Hospitals of Cleveland, Henry Wilson Payne Professor and Chairman, Department of Genetics, Case Western Reserve University School of Medicine; Director, Center for Human Genetics, University Hospitals of Cleveland, Cleveland, OH;
By (author): Roderick R. McInnes, Scientific Director, Institute of Genetics, Canadian Institutes of Health Research, Anne and Max Tanenbaum Chair in Molecular Medicine; Professor of Pediatrics and Molecular and Medical Genetics, University of Toronto and The Hospital for Sick Children, Toronto, Canada;
By (author): Robert Nussbaum, Chief, Genetic Diseases Research Branch; Acting Chief, Inherited Disease Research Branch, National Human Genome Research Institute; Executive Faculty, Johns Hopkins/NHGRI Joint Genetic Counseling Graduate program, National Institutes of Health