Buch, Englisch, 501 Seiten, Paperback, Format (B × H): 178 mm x 254 mm, Gewicht: 974 g
ISBN: 978-0-387-95046-4
Verlag: Springer
This is the fourth edition of an acclaimed introductory textbook on the structure and function of human chromosomes. The explosion of information on human genetic diseases has meant that there is a greater need than ever for students, practising physicians, laboratory technicians, and researchers to have a concise, up-to-date summary of the normal and abnormal behavior of chromosomes. This book continues to fulfill that need, and is strengthened by the complete revision of material on the molecular genetics of chromosomes and chromosomal defects.
Zielgruppe
Research
Autoren/Hrsg.
Fachgebiete
- Medizin | Veterinärmedizin Medizin | Public Health | Pharmazie | Zahnmedizin Vorklinische Medizin: Grundlagenfächer Anatomie
- Naturwissenschaften Biowissenschaften Biowissenschaften
- Medizin | Veterinärmedizin Medizin | Public Health | Pharmazie | Zahnmedizin Vorklinische Medizin: Grundlagenfächer Molekulare Medizin, Zellbiologie
- Medizin | Veterinärmedizin Medizin | Public Health | Pharmazie | Zahnmedizin Vorklinische Medizin: Grundlagenfächer Humangenetik
- Naturwissenschaften Biowissenschaften Molekularbiologie
- Naturwissenschaften Biowissenschaften Zellbiologie
Weitere Infos & Material
1 Origins and Directions of Human Cytogenetics.- 2 The Mitotic Cell Cycle.- 3 DNA Replication and Chromosome Reproduction.- 4 General Features of Mitotic Chromosomes.- 5 The Chemistry and Packaging of Chromosomes.- 6 Chromosome Bands.- 7 Molecular Correlates of Chromosome Bands.- 8 In Situ Hybridization.- 9 Main Features of Meiosis.- 10 Details of Meiosis.- 11 Meiotic Abnormalities: Abnormal Numbers of Chromosomes.- 12 Abnormal Phenotypes Due to Autosomal Aneuploidy or Polyploidy.- 13 Chromosome Structural Aberrations.- 14 The Causes of Structural Aberrations.- 15 Syndromes Due to Autosomal Deletions and Duplications.- 16 Clinical Importance of Translocations, Inversions, and Insertions.- 17 Sex Determination and the Y Chromosome.- 18 The X Chromosome, Dosage Compensation, and X Inactivation.- 19 Phenotypic Effects of Sex Chromosome Imbalance.- 20 Fragile Sites, Trinucleotide Repeat Expansion, and the Fragile X Syndrome.- 21 Euploid Chromosome Aberrations, Uniparental Disomy, and Genomic Imprinting.- 22 Chromosome Changes in Cell Differentiation.- 23 Somatic Cell Hybridization in Cytogenetic Analysis.- 24 Chromosome Instability Syndromes.- 25 DNA and Gene Amplification.- 26 Genome Destabilization and Multistep Progression to Cancer.- 27 Chromosomes and Cancer: Activation of Oncogenes.- 28 Chromosomes and Cancer: Inactivation of Tumor Suppressor Genes.- 29 Mapping Human Chromosomes.- 30 Genome Plasticity and Chromosome Evolution.- 31 The Future of Human Cytogenetics.
