eLS

eLS

Online ISBN: 9780470015902

DOI: 10.1002/047001590X

Browse by Topic

  1. Biochemistry
  2. Bioethics & Philosophy
  3. Cell Biology
  4. Developmental Biology
  5. Ecology
  6. Evolution & Diversity of Life
  7. Genetics & Disease
    1. Bioinformatics and Genetic Disease
    2. Cancer Genetics
    3. Chromosomal Disorders
    4. Epigenetics and Disease
    5. Forensic Genetics
    6. Gene and Genome Structure and Organisation
    7. Gene Expression Profiling of Genetic Disease
    8. Gene Mapping by Disease Association
    9. Gene Therapy
    10. General Genetics and Disease
    11. Genetic Counseling
    12. Genetic Models
    13. Genetics of Intelligence and Cognition
    14. Genomic Disorders
      1. Ageing Genes: Gerontogenes
      2. Anticipation
      3. Biallelic Germline Mutations of Mismatch-Repair Genes and Paediatric Malignancies
      4. Cancer: Chromosomal Abnormalities
      5. Causes and Consequences of Structural Genomic Alterations in the Human Genome
      6. Chromatin Structure and Modification: Defects
      7. Chromosomal Genetic Disease: Structural Aberrations
      8. Chromosome Instability (CIN), Aneuploidy and Cancer
      9. Comparative Genomic Hybridization in the Study of Human Disease
      10. Copy Number Variations and Neuropsychiatric Diseases
      11. DNA Repair Disorders
      12. Down Syndrome
      13. Expanding Mutations/Genetic Anticipation
      14. Fragile Sites and Human Disease
      15. Fusion Proteins and Diseases
      16. Gene Conversion in Evolution and Disease
      17. Genetic Imprinting in the Prader–Willi and Angelman Syndromes
      18. Genetics of Chromosome 22q11.2 Deletion Syndrome
      19. Genetics of Silver–Russell Syndrome
      20. Genomic and Chromosomal Instability
      21. Genomic Imprinting at the Transcriptional Level
      22. Genomic Rearrangements: Mutational Mechanisms
      23. Germline Genomic Copy Number Variation Contribution to Cancer Predisposition
      24. Hepatocellular Carcinoma
      25. Human Embryonic Aneuploidy
      26. Imprinting (Mammals)
      27. Infertility: Genetic Disorders
      28. Intellectual Disability: Genetics
      29. Microdeletion Syndromes
      30. Microdeletions and Microduplications: Mechanism
      31. MicroRNAs and Human Disease
      32. Microsatellite Instability
      33. Mismatch Repair Genes
      34. Mitochondrial Heteroplasmy and Disease
      35. Molecular Genetic Causes of Discordance in Monozygotic Twins
      36. Molecular Genetics of Incontinentia Pigmenti
      37. Molecular Genetics of Mental Retardation
      38. Molecular Genetics of Myelodysplastic Syndromes
      39. Molecular Genetics of Rhabdomyosarcoma
      40. Molecular Genetics of Spermatogenic Disturbances
      41. Molecular Genetics of Williams–Beuren Syndrome
      42. Molecular Mechanisms Underlying Pathogenic Missense Mutations
      43. You have free access to this content
        Monosomies
      44. Mosaicism
      45. Non-B DNA Structure and Mutations Causing Human Genetic Disease
      46. Noncoding RNAs in Biology and Disease
      47. Numerical Chromosomal Aberrations in Human Diseases
      48. Origins of Human Aneuploidy
      49. Polyploidy
      50. Pseudoautosomal Inheritance
      51. Relevance of Copy Number Variation to Human Genetic Disease
      52. Repetitive Elements and Human Disorders
      53. Retrotransposons and Human Disease
      54. Schizophrenia and 22q11.2 Deletion Syndrome
      55. Segmental Duplications and Genetic Disease
      56. Sex Chromosome Abnormalities
      57. Somatic Genome Variations
      58. Sotos Syndrome
      59. Spontaneous Function Correction of Pathogenic Alleles in Inherited Diseases Resulting in Somatic Mosaicism
      60. SRY, Sex Determination and Gonadal Differentiation
      61. Studying Genomic Aberrations by Microarray Profiling
      62. Tandem Repeat Instability and Genome Evolution
      63. Translocation Breakpoints in Cancer
      64. Transposons as Natural and Experimental Mutagens
      65. You have free access to this content
        Trisomy
      66. Uniparental Disomy
      67. Uniparental Disomy in Cancer – A New Tool in Molecular Cancer
      68. X-Chromosome Inactivation
      69. X-chromosome Inactivation and Disease
      70. XYY Syndrome
      71. Y-chromosome-linked Traits
    15. Inter-Individual Variation and Polymorphism
    16. Linkage Analysis
    17. Mitochondrial Diseases
    18. Model Organisms and Human Disease
    19. Molecular Genetics of Common and Complex Disease
    20. Mutational Mechanisms of Genetic Disease
    21. Pharmacogenetics and Pharmacogenomics
    22. Proteomic Studies of Genetic Disease
    23. Quantitative Genetics
    24. Specific Genetic Disorders
    25. Statistical Methodology in Genetics
    26. Techniques and Tools in Clinical Genetics
  8. Immunology
  9. Microbiology
  10. Molecular Biology
  11. Neuroscience
  12. Plant Science
  13. Science & Society
  14. Structural Biology
  15. Virology

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